openSNP

New Publication

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
lusterdallama	9288	8306	15.12.2019 02:58
elliothyc	9287	8305	15.12.2019 00:16
Kdd9882	9286	8304	14.12.2019 21:19
MikeABarry	9285	8303	14.12.2019 18:58
malcomb	9284	8302	14.12.2019 05:51
GHAMM	9283	8301	13.12.2019 18:20
A22B98A37R	9282	8300	13.12.2019 13:47
Cheryl L Alford	9281	8299	13.12.2019 00:44
Anthony Youngblood	9280	8298	12.12.2019 19:20
emily	9279	8297	12.12.2019 19:01
Tgirl	9278	8296	12.12.2019 15:21
Frank	9277	8295	12.12.2019 07:37
iklili	9276	8294	12.12.2019 03:55
Genomica	9275	8293	11.12.2019 12:53
chet	9274	8292	11.12.2019 12:23
milchkuh	9273	8291	11.12.2019 09:27
sywang	9272	8290	11.12.2019 05:20
kirillshorin	9271	8289	10.12.2019 22:03
Godwin86	9270	8288	10.12.2019 09:11
juliekelts	9269	8287	10.12.2019 04:02

Show All Users

New genotypes

Uploaded by	#	Genotype-ID	Uploaded on
DeathFeast	5451	7611	15.12.2019 18:14	Description	Download
lusterdallama	5450	7609	15.12.2019 03:13	Description	Download
elliothyc	5449	7608	15.12.2019 00:18	Description	Download
Kdd9882	5448	7607	14.12.2019 21:19	Description	Download
malcomb	5447	7606	14.12.2019 05:52	Description	Download
GHAMM	5446	7605	13.12.2019 18:23	Description	Download
A22B98A37R	5445	7603	13.12.2019 13:48	Description	Download
Cheryl L Alford	5444	7602	13.12.2019 00:45	Description	Download
emily	5443	7599	12.12.2019 19:02	Description	Download
Aether	5442	7598	12.12.2019 15:44	Description	Download
Tgirl	5441	7597	12.12.2019 15:29	Description	Download
Frank	5440	7596	12.12.2019 07:37	Description	Download
iklili	5439	7595	12.12.2019 03:56	Description	Download
chet	5438	7593	11.12.2019 12:24	Description	Download
Godwin86	5437	7591	10.12.2019 09:12	Description	Download
pabickwermert	5436	7590	09.12.2019 06:54	Description	Download
kcmom	5435	7588	08.12.2019 22:40	Description	Download
nmarta131	5434	7587	08.12.2019 15:48	Description	Download
hazelgrace	5433	7586	07.12.2019 03:57	Description	Download
Enrique	5432	7585	06.12.2019 23:10	Description	Download

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Phenotypes

Name	Variations	# of Users
black hair and brown eyes, blood B+, 6,5 tall	Caucasian	1
Tattoos	Yes-20 0	5
Birthing pain	Yes-9	1
Allergic to bees	Epi pen allergic Not allergic	3
Wake time before leaving for work	2 hours 1 hour	3
Allergic to a steroid shot	Yes- kenalog Don't know	2
High kidneys	Yes No	2
Have a military neck	Yes No	4
nail biter, lip biter or skin picker when stressed	Lip and skin No	2
Alcoholism	27-2 Alcohol dependent	2
Can you wake up at night, drink coffee and a couple hours later go right back to sleep	Yes No	2
Do you read a lot on the why’s and how’s things work.	Yes	3
Deep Blue	Blue blonde ginger eyes hair albinism mcr1 blindness strabismus retinis pigmentosa musician's dystonia Not blue eyes	2
abnormal brain shape	Right side of cerebellum and occipital lobe markedly smaller than left side. None known	2
immunological disorder: HLA-b27	Reiter's syndrome None	2
RCCX	Multiple confirmed diagnosis None	2
Feel that intelligence is genetically more than just IQ	Feel that intelligence is more than just iq, don't feel that intelligence is genetically more than just iq	2
Strongly feel that true "intelligence" is more than just IQ	Strongly feel that intelligence is genetically more than just iq.	8
Chimera or mosaic?	Yes Mosaic	3
Reading speed(WPM)	381 600	3

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SNP comments

Comment by	Subject	Date	SNP
might_be_bulma	Who's down with SNP....yeah, I'm CG	28.10.2019 23:40	rs13078881
jwater148	RCCX Theory - EDS/ADHD/POTS	25.07.2019 06:27	rs1009382
perelgut	I'm TT and obese	05.06.2019 14:20	rs9939609
00RHZ2Sap2	Analysis	02.06.2019 21:39	rs2294008
Denatonium	-	28.03.2019 20:37	rs10187368
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

Phenotypes comments

Comment by	Phenotype	Subject	Date
Paul Shenton	black hair and brown eyes, blood B+, 6,5 tall	That is not a phenotype.	21.10.2019 20:35
James Francies	Hair and eye color Brown	Eye color	08.09.2019 08:55
GreenStar	Squizophrenia	This is not a legitimate question.	08.08.2019 07:58
GreenStar	Rythm Test Result	Please correct the spelling on this.	08.08.2019 07:45
Bill Aldrich	Response to Enbrel	Enbrel mildly ineffective	20.07.2019 16:15
McTrimm	Political Ideology	What Idiot?	12.05.2019 20:38
MP	Are you a map lover?	My map lover answer	27.03.2019 18:31
MP	MENSA Member	Mensa	27.03.2019 18:28
Dolphin	Missing canine teeth	Missing canine teeth	26.02.2019 18:58
Dolphin	Missing canine teeth	Provide how many canine teeth you are missing	26.02.2019 18:58
Dolphin	Missing canine teeth	Provide how many canine teeth you are missing	26.02.2019 18:58
Brian Pardy	Light-skinned, European Ancestry (rs14256654)	rs1426654, not rs14256654	26.02.2019 18:42
stephen bradley	Number of wisdom teeth	0 wisdom teeth	06.01.2019 08:42
Gollaher@gmail.com	Synesthesia	How do I answer?	02.01.2019 04:45
TamiBryGWI	Post traumatic Stress Disorder or PTSD?	Rs1800629	03.12.2018 21:57
DJValkyrie	Kell Blood Group (K/k antigens)	-	26.11.2018 05:51
DJValkyrie	Migraine frequency	Topamax	26.11.2018 02:38
DJValkyrie	Age you started wearing glasses	Strabismus in addition to myopia	26.11.2018 01:51
Clove1008	SLE - Lupus	I think I do	21.11.2018 03:57
Philippe Henry	Affinity to Cannabis	The genetic basis of the human-cannabis relationship	09.11.2018 05:14

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New Publication

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New genotypes

Phenotypes

SNP comments

Phenotypes comments

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