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New Publication Rss

Author Title Found at SNPs
J. Yang FTO genotype is associated with phenotypic variability of body mass index 21.05.2014 10:47 rs7202116
J Yang FTO genotype is associated with phenotypic variability of body mass index 21.05.2014 10:47 rs7202116
Jian Yang FTO genotype is associated with phenotypic variability of body mass index 21.05.2014 10:47 rs7202116
Jian Yang FTO genotype is associated with phenotypic variability of body mass index 21.05.2014 10:47 rs7202116
Yannick Allanore Genome-Wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis 21.05.2014 10:33 rs6457617
Richard Sherva Evidence for a QTL affecting low levels of apolipoprotein B and low-density lipoprotein on chromosome 10 in Caucasian families 21.05.2014 07:49 rs2277205
Richard Sherva Evidence for a quantitative trait locus affecting low levels of apolipoprotein B and low density lipoprotein on chromosome 10 in Caucasian families. 21.05.2014 07:49 rs2277205
Vinay Singh Tanwar Common variant in FUT2 gene is associated with levels of vitamin B12 in Indian population 21.05.2014 07:22 rs602662
Tiziana Larussa High prevalence of polymorphism and low activity of thiopurine methyltransferase in patients with inflammatory bowel disease 21.05.2014 07:13 rs1800462
L Christie Rockwell Worldwide distribution of allelic variation at the progesterone receptor locus and the incidence of female reproductive cancers. 21.05.2014 05:38 rs10895068
B Kelmendi Association of polymorphisms in HCN4 with mood disorders and obsessive compulsive disorder 21.05.2014 05:28 rs498005
Kentaro Mizuno Single-nucleotide polymorphism in wt1 gene in a hyperplastic intralobar nephrogenic rest with botryoid protrusion 21.05.2014 05:12 rs16754
Frederik Damm ID1 expression associates with other molecular markers and is not an independent prognostic factor in cytogenetically normal acute myeloid leukaemia. 21.05.2014 05:12 rs16754
Xingru Li Single Nucleotide Polymorphisms in the Wilms' Tumour Gene 1 in Clear Cell Renal Cell Carcinoma 21.05.2014 05:12 rs16754
Darat Lauhakirti WT1 mutations and polymorphisms in Southeast Asian acute myeloid leukemia 21.05.2014 05:12 rs16754
Frederik Damm Integrative prognostic risk score in acute myeloid leukemia with normal karyotype 21.05.2014 05:12 rs16754
Alexander P. Reiner Genome-Wide association study of white blood cell count in 16,388 african americans: The continental Origins and Genetic Epidemiology network (COGENT) 21.05.2014 03:47 rs9131
Edna Gr??nblatt Genetic variation in the choline O-acetyltransferase gene in depression and Alzheimer's disease: The VITA and Milano studies 21.05.2014 03:47 rs1880676
Sangmee Ahn Jo ApoE-?? 4-dependent association of the choline acetyltransferase gene polymorphisms (2384G>A and 1882G>A) with Alzheimer's disease 21.05.2014 03:47 rs1880676
X Tan Genetic variation in the GSTM3 promoter confer risk and prognosis of renal cell carcinoma by reducing gene expression. 21.05.2014 03:22 rs7483
Camilo Gómez-Garzón A genome-scale metabolic reconstruction of Lysinibacillus sphaericus unveils unexploited biotechnological potentials 15.05.2018 08:42 rs15750
José Inácio Salles Vascular Endothelial Growth Factor Receptor-2 Polymorphisms Have Protective Effect against the Development of Tendinopathy in Volleyball Athletes 15.05.2018 08:10 rs1570360
Agnieszka Paradowska-Gorycka Relationship between VEGF Gene Polymorphisms and Serum VEGF Protein Levels in Patients with Rheumatoid Arthritis 15.05.2018 08:10 rs1570360
Michael W. Nagle The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane 15.05.2018 07:04 rs1564282
Kathrin Landgraf FTO Obesity Risk Variants Are Linked to Adipocyte IRX3 Expression and BMI of Children - Relevance of FTO Variants to Defend Body Weight in Lean Children? 15.05.2018 06:04 rs1558902
Mette Korre Andersen Identification of Novel Genetic Determinants of Erythrocyte Membrane Fatty Acid Composition among Greenlanders 15.05.2018 04:36 rs1551304
Xiuju Li Stop Codon Polymorphisms in the Human SLC9A1 Gene Disrupt or Compromise Na+/H+ Exchanger Function 14.05.2018 23:21 rs150618776
Sze Ling Chan Association and clinical utility of NAT2 in the prediction of isoniazid-induced liver injury in Singaporean patients 14.05.2018 20:54 rs1495741
Anne-Laure Renault ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry 14.05.2018 20:42 rs1494961
Lara Marrone Generation of iPSCs carrying a common LRRK2 risk allele for in vitro modeling of idiopathic Parkinson's disease 14.05.2018 20:00 rs1491923
Mustafa M. Munye COLEC10 is mutated in 3MC patients and regulates early craniofacial development 14.05.2018 19:34 rs149010496
Mala Pande Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies 14.05.2018 15:57 rs4939827
Abdou Mousas Rare coding variants pinpoint genes that control human hematological traits 14.05.2018 14:09 rs146597587
Po-Yu Yang Impact of Maspin Polymorphism rs2289520 G/C and Its Interaction with Gene to Gene, Alcohol Consumption Increase Susceptibility to Oral Cancer Occurrence 14.05.2018 11:55 rs1455555
Luca A. Lotta Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis 14.05.2018 08:13 rs1440581
Jan Rehker Caspase-8, association with Alzheimer’s Disease and functional analysis of rare variants 14.05.2018 06:34 rs143332484
Bhoom Suktitipat Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome 14.05.2018 04:43 rs142644288
Dirk Smith A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma 14.05.2018 02:57 rs146597587 rs1420101
Ai-Ru Hsieh A non-threshold region-specific method for detecting rare variants in complex diseases 14.05.2018 00:14 rs1408705
Maria Delio Development of a Targeted Multi-Disorder High-Throughput Sequencing Assay for the Effective Identification of Disease-Causing Variants 13.05.2018 22:44 rs140252282

Users

Name ID # Joined on
Standard head kgib0198 7910 7063 22.09.2018 21:58
Standard head Nasty33 7909 7062 22.09.2018 16:36
Standard head Alex 7908 7061 22.09.2018 14:51
Standard head Stephen martin 7907 7060 22.09.2018 04:24
Standard head Ron 7906 7059 22.09.2018 02:47
Standard head alicesusandeexx 7905 7058 21.09.2018 22:42
Standard head ghardin 7904 7057 21.09.2018 20:24
Standard head Andrea 7903 7056 21.09.2018 10:52
Standard head hoza1 7902 7055 20.09.2018 10:20
Standard head Mielikki 7901 7054 19.09.2018 19:12
Standard head Alexey 7900 7053 19.09.2018 18:49
Standard head cawloid 7899 7052 18.09.2018 18:47
Standard head david heldreth 7898 7051 18.09.2018 16:22
Standard head lmairesse 7897 7050 18.09.2018 15:52
Standard head Elisephipps 7896 7049 18.09.2018 13:46
Standard head csabai 7895 7048 18.09.2018 13:37
Standard head Ginax89 7894 7047 18.09.2018 05:06
Standard head domingos 7893 7046 17.09.2018 21:59
Standard head scubaberman 7892 7045 17.09.2018 21:40
Standard head rlhornsby 7891 7044 17.09.2018 19:44
Show All Users

New genotypes Rss

Uploaded by # Genotype-ID Uploaded on
Standard head kgib0198 4625 6256 22.09.2018 22:02 Description Download
Standard head Nasty33 4624 6255 22.09.2018 16:38 Description Download
Standard head Alex 4623 6254 22.09.2018 14:52 Description Download
Standard head Stephen martin 4622 6253 22.09.2018 04:28 Description Download
Standard head alicesusandeexx 4621 6252 22.09.2018 01:14 Description Download
Standard head ghardin 4620 6250 21.09.2018 20:25 Description Download
Standard head hoza1 4619 6249 20.09.2018 10:22 Description Download
Standard head Mielikki 4618 6248 19.09.2018 19:13 Description Download
Standard head Alexey 4617 6247 19.09.2018 18:51 Description Download
Standard head cawloid 4616 6246 18.09.2018 18:49 Description Download
Standard head david heldreth 4615 6245 18.09.2018 16:23 Description Download
Standard head lmairesse 4614 6244 18.09.2018 15:57 Description Download
Standard head Ginax89 4613 6243 18.09.2018 05:07 Description Download
Standard head scubaberman 4612 6241 17.09.2018 21:40 Description Download
Standard head BlackOmega 4611 6239 16.09.2018 22:01 Description Download
Standard head Kristina 4610 6238 16.09.2018 03:13 Description Download
Standard head Carly45 4609 6237 14.09.2018 15:10 Description Download
Standard head johnanderson137 4608 6236 13.09.2018 15:15 Description Download
Standard head Kate 4607 6235 13.09.2018 02:30 Description Download
Standard head Klevine 4606 6234 12.09.2018 23:56 Description Download
Show All Genotypes

Phenotypes

Name Variations # of Users
Gorlin sign
  • Yes i do have the ability to touch the tip of my nose with my tongue
  • No
3
Skin color.
  • Yellowish hue to my fair skin, maybe slightly olive. white though. do tan overall
  • Fair-medium. white with some ability to burn.
4
GREEK DNA
  • Greek
1
Eye Color - Heterochromia
  • Yes
  • No.
5
black skin,O+,hair Black,Eye color Brown,
  • Hair color started about 19 yrs old graying
  • No
3
Rosacea
  • Yes, papulopustular rosacea
  • No, don't have it
3
Suicidality
  • Anxitey, ptsd, major depression without suicidal ideation
  • Never even thought about suicide
6
Fibromyalgia Response to SRI drugs
  • Do not work for fibromyalgia or depressive issues.
  • Does not apply to me
  • They work but cause sexual side effects and some numbing of emotions
3
Response to Codeine
  • No relief, intense itch, not id'd by testing
  • No relief - same with vicodin and morphine
  • No relief at all
  • Works as intended
7
Optimistic, empathetic, handles stress well
  • Rs53576 g/g reading the emotion of others, be optimistic
  • Rs53576
  • Handle situations very well in chaotic times
  • No
9
Sleep duration
  • 5.5 hours
  • Rs11046205
  • 6.5 hour
4
Severe Acne
  • No
  • Was treated for acne for years (teens), but derm diagnosed as rosacea (adult)
  • Mild hormonal acne
7
dark Blonde,fair skin,brown eyes
  • Blonde,white
1
Extra Teeth
  • Yes
  • Had all four wisdom teeth. a grandfather had extra teeth.
3
Familial hypercholesterolemia
  • Above 400 without meds
1
Dark brown,Rheusus Neg B,Olive
  • Dark brown, caucasian
1
Lichen Sclerosis(LS)/Balanitis Xerotica Obliterates(BXO)
  • Yes
  • I dont have this
4
Force
  • "luke, i am your father"
  • Hello hello hello!? is there anybody in there?
4
Sang À+
  • Caucasian
3
Cushing's Disease
  • Diagnosed
  • No
  • No, but my mom had it
7
Show All Phenotypes

SNP comments

Comment by Subject Date SNP
Vikki Stefans re rs151242451 24.07.2018 21:27 rs151242451
Lucie Franklin Leduc - 10.07.2018 15:30 rs2032582
ckova T/T 18.04.2018 09:07 rs9939609
Jennifer L. G. - 13.04.2018 06:15 rs76763715
SatoriFound Treatment response 14.02.2018 01:16 rs8099917
SatoriFound Treatment response 14.02.2018 01:13 rs12979860
asheskye Wrong finding, opposite effect. CC polymorphic genotype is associated with a decreased risk of BC 18.11.2017 05:00 rs11614913
dooptydoop Are there any c/t or t/t people who are sleepy all the time? 05.07.2017 22:43 rs73598374
Raffeil - 19.05.2017 00:50 rs369202065
R I'm very skinny also. 24.08.2016 14:09 rs9939609
Jennifer L. G. - 01.12.2014 21:35 rs10512985
ett-1 rs289741(GG) and rs5882(GG) 22.01.2014 07:00 rs289741
Couscous Nomad - 10.06.2013 22:53 rs16969968
Couscous Nomad - 10.06.2013 20:39 rs3212041
Linda Bique CG at this SNP as well 05.01.2013 14:12 rs13078881
E. Campbell Genotype CCAT 17.09.2012 16:51 rs34983651
E. Campbell D and I genotype? 17.09.2012 16:40 rs8176719
E. Campbell Genotype CT 17.09.2012 16:02 rs34442879
E. Campbell Genotype CT 17.09.2012 15:58 rs17355460
E. Campbell Genotype AG 17.09.2012 13:55 rs1695

Phenotypes comments

Comment by Phenotype Subject Date
Denatonium Squizophrenia - 02.09.2018 02:53
Denatonium Synesthesia - 01.09.2018 20:05
Philippe Henry Affinity to Cannabis a tweet about it 19.03.2018 13:33
Philippe Henry Affinity to Cannabis see where you match up 19.03.2018 12:12
Philippe Henry Affinity to Cannabis Want to see how you match up 19.03.2018 12:12
DemonRaven Sexual Preferences I love how no one reads the entire thing. 13.01.2018 18:09
Margaret Ruth Frink Score on Big Five at PersonalityLab.org How do I edit my entry? 04.01.2018 11:12
Paul Shenton Cusp of Carabelli Failed idea 18.11.2017 19:06
Anaro Lexnon Hemochromotosis wiki link 19.06.2017 11:56
markanini Chest Pain on Ritalin - 18.06.2017 11:27
J Smith Have You Been Diagnosed With Brown's Syndrome (Tendon Sheath Syndrome)? wrong answer 14.03.2017 03:23
a_burriesci91 Adult Second Language Acquistion Aptitude - 01.01.2017 03:03
a_burriesci91 Number of wisdom teeth - 01.01.2017 02:42
a_burriesci91 ring finger longer than index finger - 01.01.2017 02:35
James Biehl Neanderthal (Interpretome) How to get this data? 27.12.2016 19:29
Jonathan Day Autism Problem with autism 28.11.2016 00:04
Paul Shenton FBN1 Mutation Not a phenotype. Extremely useless. 09.02.2016 03:29
kell Pectus Excavatum (sunken chest) Pectus Excavatum (sunken chest) 08.02.2016 23:08
kell paternal or Y haplogroup G1a 08.02.2016 21:28
Paul Shenton maternal or mTDNA haplogroup One of the least well though out questions. 25.12.2015 18:14