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
Mauro	9429	8429	17.02.2020 04:53
Shae_Clark	9428	8428	17.02.2020 01:09
P	9427	8427	15.02.2020 21:09
GeneSplicer	9426	8426	13.02.2020 04:22
AVSD	9424	8425	12.02.2020 20:47
indigolotus2@outlook.com	9422	8424	08.02.2020 19:23
sqpaa	9421	8423	08.02.2020 19:04
seankettle	9418	8422	06.02.2020 21:30
Oleg	9417	8421	06.02.2020 16:48
Merryh	9416	8420	06.02.2020 14:38
cuneytg	9415	8419	06.02.2020 13:21
Doodlebop246	9414	8418	05.02.2020 22:13
Omicron	9413	8417	05.02.2020 21:47
LORETTA	9412	8416	05.02.2020 19:12
José Antonio	9411	8415	03.02.2020 15:49
Darrenburnett	9410	8414	03.02.2020 13:08
aejurgensen	9409	8413	02.02.2020 01:28
dbledble	9408	8412	01.02.2020 15:17
Chiara Sgro	9407	8411	01.02.2020 08:30
sacredpens	9406	8410	01.02.2020 01:40

Show All Users

New genotypes

Uploaded by	#	Genotype-ID	Uploaded on
Mauro	5514	7728	17.02.2020 04:55	Description	Download
Shae_Clark	5513	7727	17.02.2020 01:10	Description	Download
AVSD	5512	7725	12.02.2020 20:48	Description	Download
indigolotus2@outlook.com	5511	7722	08.02.2020 19:24	Description	Download
sqpaa	5510	7721	08.02.2020 19:05	Description	Download
seankettle	5509	7718	06.02.2020 21:33	Description	Download
Oleg	5508	7717	06.02.2020 16:49	Description	Download
Doodlebop246	5507	7716	05.02.2020 22:15	Description	Download
Omicron	5506	7715	05.02.2020 21:49	Description	Download
LORETTA	5505	7714	05.02.2020 19:19	Description	Download
jennifermartin8	5504	7713	03.02.2020 21:05	Description	Download
Darrenburnett	5503	7711	03.02.2020 13:09	Description	Download
dbledble	5502	7709	01.02.2020 15:18	Description	Download
sacredpens	5501	7708	01.02.2020 01:44	Description	Download
bitsy	5500	7707	01.02.2020 01:12	Description	Download
Mturitz	5499	7706	31.01.2020 15:34	Description	Download
Mturitz	5498	7705	31.01.2020 15:30	Description	Download
atlantic97	5497	7704	30.01.2020 23:19	Description	Download
mc0536908	5496	7703	30.01.2020 19:09	Description	Download
Andrea	5495	7702	30.01.2020 00:23	Description	Download

Show All Genotypes

Phenotypes

Name	Variations	# of Users
Wiggle My Ears	Brunette Can wiggle ears, blue eyes	3
tourettes syndrome	F no Yes	4
repetitive movements or unwanted sounds	No	2
The Cracker Test	23	2
Which is the cheapest country to study MBBS?	Mbbs in ukraine Russia	3
Why MBBS Ukraine Is The Best Option For MBBS Aspirants?	Mbbs in ukraine Enter your phenotype:? better you take off.... ok!!	3
Simian Line(s)	Double simian No on either hand.	3
black hair and brown eyes, blood B+, 6,5 tall	Caucasian	2
Tattoos	Yes-20 0	7
Birthing pain	Yes-9	2
Allergic to bees	Epi pen allergic Not allergic	6
Wake time before leaving for work	2 hours 1 hour	4
Allergic to a steroid shot	Yes- kenalog Don't know	3
High kidneys	Yes No	3
Have a military neck	Yes No	6
nail biter, lip biter or skin picker when stressed	Lip and skin No	3
Alcoholism	27-2 Alcohol dependent None	4
Can you wake up at night, drink coffee and a couple hours later go right back to sleep	Yes No	4
Do you read a lot on the why’s and how’s things work.	Yes	4
Deep Blue	Blue blonde ginger eyes hair albinism mcr1 blindness strabismus retinis pigmentosa musician's dystonia Not blue eyes	3

Show All Phenotypes

SNP comments

Comment by	Subject	Date	SNP
Aternias	I am A/A and have Tourette’s Syndrome.	29.01.2020 04:50	rs7868992
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

Phenotypes comments

Comment by	Phenotype	Subject	Date
DigiGirlFL	Ability to Tan	-	20.01.2020 03:47
Anaro Lexnon	Reading speed(WPM)	I tested at	14.01.2020 15:28
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

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