Updates

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 cmhong68 7692 6861 20.07.2018 12:36
Standard head tandjhayes918 7691 6860 20.07.2018 09:35
Standard head Samantha Chappell 7689 6859 19.07.2018 23:47
Img 0554 sdaigle318 7688 6858 19.07.2018 20:32
Standard head dimitri 7687 6857 19.07.2018 10:15
Standard head aleene 7686 6856 19.07.2018 08:01
Standard head 2redhot 7685 6855 18.07.2018 21:20
Standard head Jenn 7684 6854 18.07.2018 15:09
Girl running kimron 7683 6853 18.07.2018 12:58
Standard head gbiotx 7682 6852 18.07.2018 11:02
Standard head Bert Fletcher 7681 6851 17.07.2018 23:23
Standard head bigk1260 7680 6850 17.07.2018 21:33
Standard head Daniela Vergara 7679 6849 17.07.2018 21:05
Standard head john 7678 6848 17.07.2018 20:35
Standard head Zed 7677 6847 17.07.2018 02:05
Standard head jnickelljr 7676 6846 17.07.2018 01:09
Standard head ltlist 7675 6845 16.07.2018 12:10
Face blargle 7674 6844 16.07.2018 07:09
Standard head Daemonette 7673 6843 16.07.2018 06:35
Standard head frank 7672 6842 16.07.2018 01:25
Show All Users

New genotypes Rss

Uploaded by # Genotype-ID Uploaded on
Standard head tandjhayes918 4471 6036 20.07.2018 15:01 Description Download
Standard head tandjhayes918 4470 6035 20.07.2018 09:36 Description Download
Standard head Grebnaws 4469 6034 20.07.2018 04:31 Description Download
Img 0554 sdaigle318 4468 6032 19.07.2018 20:33 Description Download
Standard head dimitri 4467 6031 19.07.2018 10:18 Description Download
Standard head 2redhot 4466 6030 18.07.2018 21:23 Description Download
Standard head Jenn 4465 6029 18.07.2018 15:10 Description Download
Mikes%20eye Aussie 4464 6028 18.07.2018 05:41 Description Download
Standard head john 4463 6025 17.07.2018 20:36 Description Download
Standard head Zed 4462 6024 17.07.2018 02:06 Description Download
Standard head jnickelljr 4461 6023 17.07.2018 01:10 Description Download
Standard head ltlist 4460 6022 16.07.2018 12:15 Description Download
Face blargle 4459 6021 16.07.2018 07:10 Description Download
Standard head frank 4458 6020 16.07.2018 01:26 Description Download
Standard head telltheirstories 4457 6019 15.07.2018 23:31 Description Download
Standard head jamesjlee29 4456 6018 15.07.2018 22:00 Description Download
Standard head Irene Macdonald 4455 6010 15.07.2018 06:29 Description Download
Standard head limaecho 4454 6009 14.07.2018 22:07 Description Download
Standard head Ax 4453 6008 14.07.2018 21:19 Description Download
Standard head Maisie 4452 6007 14.07.2018 02:17 Description Download
Show All Genotypes

Phenotypes

Name Variations # of Users
Suicidality
  • Anxitey, ptsd, major depression without suicidal ideation
  • Never even thought about suicide
2
Fibromyalgia Response to SRI drugs
  • Do not work for fibromyalgia or depressive issues.
  • Does not apply to me
2
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
4
Optimistic, empathetic, handles stress well
  • Rs53576
  • Handle situations very well in chaotic times
  • No
  • Rs53576 g/g reading the emotion of others, be optimistic
6
Sleep duration
  • Rs11046205
  • 6.5 hour
  • 5.5 hours
3
Severe Acne
  • No
2
dark Blonde,fair skin,brown eyes
  • Blonde,white
1
Extra Teeth
  • Yes
2
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?
3
Sang À+
  • Caucasian
2
Cushing's Disease
  • Diagnosed
  • No
  • No, but my mom had it
6
Horseshoe kidney
  • Present
  • None
5
No Allergies
  • No allergies
  • Rhinitis (seasonal)
10
Hazel Eyes
  • Hazel
  • Blue
  • Green
15
clubfoot
  • Clubfoot present at birth
  • No
7
Hypospadias
  • Yes
  • Partially, the hole is not on the underside, but close.
  • No
7
brown hair colour, white skin color
  • Caucasian
  • Yes
6
Show All Phenotypes

SNP comments

Comment by Subject Date SNP
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
mike Warning C->G and T->A 10.09.2012 13:44 rs25531

Phenotypes comments

Comment by Phenotype Subject Date
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
Paul Shenton paternal or Y haplogroup One of the least thought out questions 25.12.2015 18:13
Anaro Lexnon Allergy to artificial grape flavoring Which chemical is this? 05.08.2015 12:10