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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 NICH314 7494 6688 21.05.2018 09:31
Standard head Laticia 7493 6687 21.05.2018 05:12
Standard head rpique 7491 6686 20.05.2018 17:37
Standard head mike 7490 6685 20.05.2018 08:05
Standard head Andrea 7489 6684 19.05.2018 11:51
Standard head BooHoosier 7488 6683 19.05.2018 07:22
Standard head CLafuente1983 7487 6682 19.05.2018 02:26
Standard head FiFiMontgomery 7485 6681 18.05.2018 04:47
Standard head b17flygirl 7484 6680 17.05.2018 05:05
Standard head Abbad Alharbi 7483 6679 16.05.2018 23:35
Standard head morganmarch 7481 6678 16.05.2018 18:39
Standard head kenkhan 7480 6677 16.05.2018 15:06
Standard head RoachQ 7479 6676 16.05.2018 08:55
Standard head EW 7478 6675 16.05.2018 05:15
Standard head djlevy 7477 6674 16.05.2018 02:22
Standard head evaaa 7476 6673 15.05.2018 22:48
Standard head dottie78161 7475 6672 15.05.2018 16:08
Standard head Nicola 7474 6671 15.05.2018 14:52
Standard head Ariadni 7473 6670 15.05.2018 07:37
Standard head chris.koll 7472 6669 15.05.2018 06:47
Show All Users

New genotypes Rss

Uploaded by # Genotype-ID Uploaded on
Standard head mike 4333 5837 20.05.2018 08:06 Description Download
Standard head BooHoosier 4332 5835 19.05.2018 07:23 Description Download
Standard head CLafuente1983 4331 5834 19.05.2018 02:50 Description Download
Standard head CLafuente1983 4330 5833 19.05.2018 02:30 Description Download
Standard head FiFiMontgomery 4329 5830 18.05.2018 05:08 Description Download
Standard head b17flygirl 4328 5829 17.05.2018 05:07 Description Download
Standard head Abbad Alharbi 4327 5828 16.05.2018 23:37 Description Download
Standard head morganmarch 4326 5826 16.05.2018 18:40 Description Download
Standard head kenkhan 4325 5825 16.05.2018 15:08 Description Download
Standard head EW 4324 5823 16.05.2018 05:16 Description Download
Westr 178kb Westr 4323 5822 15.05.2018 17:55 Description Download
Standard head dottie78161 4322 5821 15.05.2018 16:14 Description Download
Standard head Nicola 4321 5820 15.05.2018 14:53 Description Download
Standard head chris.koll 4320 5819 15.05.2018 06:48 Description Download
Standard head ilanso 4319 5818 14.05.2018 22:49 Description Download
12672190 10153573433417585 1773071000947199233 o %282017 03 05 03 53 33 utc%29 cparker354 4318 5817 14.05.2018 21:06 Description Download
Standard head aimee.burnett 4317 5816 14.05.2018 19:26 Description Download
Standard head Antoinette Pomerantz 4316 5815 14.05.2018 06:28 Description Download
Standard head Brazzen1 4315 5814 14.05.2018 02:31 Description Download
Standard head MSteinhelfer 4314 5813 14.05.2018 00:11 Description Download
Show All Genotypes

Phenotypes

Name Variations # of Users
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
 3
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
 5
Horseshoe kidney
  • Present
  • None
 3
No Allergies
  • No allergies
  • Rhinitis (seasonal)
 8
Hazel Eyes
  • Hazel
  • Blue
  • Green
 12
clubfoot
  • Clubfoot present at birth
  • No
 6
Hypospadias
  • Yes
  • Partially, the hole is not on the underside, but close.
  • No
 6
brown hair colour, white skin color
  • Caucasian
  • Yes
 4
Ocular migraines
  • Yes
  • No
 5
blue eyes with yellow stripes making them look depending on the light or my mood
  • fair skin with freckles, dark blonde
  • No
 6
Score on Big Five at PersonalityLab.org
  • Ex67, ag58, co27, nu42, op100
  • Ex48, ag90, co67, ne25, op77
  • Ag54, co75, ne85, op96
  • Ex15, ag42, co46, nu88, op60
  • Ex44, ag85, co40, ne77, op98
  • Ex62, ag96, co92, ne21, op94
  • Ex33, ag73, co62, ne38, op88
  • Ex31, ag89, co75, ne29, op88
 8
hemophilia C (factor XI deficiency is caused by "rare mutations" in the F11 gene)
  • Tonsillectomy
  • None
 4
Do you prefer python, matlab, or R?
  • Python
  • Python & r
  • R
  • None
 5
Pain Tolerance
  • High
  • Depends on the kind of pain
  • Very high
  • Low
 17
inverted nipples
  • Yes - both
  • None
 13
Show All Phenotypes

SNP comments

Comment by Subject Date SNP
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
mike LHON VISUAL LOSS 10.09.2012 12:22 i5000099

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

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