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
l2wisp	12088	10852	25.09.2023 15:30
Spencer	12087	10851	24.09.2023 22:36
LauraM	12086	10850	24.09.2023 19:01
zrejali98	12085	10849	24.09.2023 12:28
michaela	12084	10848	24.09.2023 00:29
DIPTANIL	12083	10847	23.09.2023 13:46
Claudia	12082	10846	23.09.2023 12:10
Matuomala	12081	10845	22.09.2023 18:38
guillaume	12080	10844	22.09.2023 10:16
ErinRumpke	12079	10843	22.09.2023 03:35
laurandzis	12078	10842	22.09.2023 00:34
leonan0	12077	10841	21.09.2023 19:57
hart92	12076	10840	21.09.2023 19:05
heuristiclynx	12075	10839	19.09.2023 13:54
veda foxtrot	12073	10838	18.09.2023 19:04
hjwil132	12072	10837	18.09.2023 17:54
Wingidthing	12071	10836	17.09.2023 06:46
krystalpromise	12070	10835	17.09.2023 05:48
Artil	12069	10834	17.09.2023 05:14
claire	12068	10833	17.09.2023 00:55

Show All Users

New genotypes

Uploaded by	#	Genotype-ID	Uploaded on
l2wisp	6856	9954	25.09.2023 15:32	Description	Download
LauraM	6855	9953	24.09.2023 19:02	Description	Download
Claudia	6854	9951	23.09.2023 12:13	Description	Download
Claudia	6853	9950	23.09.2023 12:11	Description	Download
Matuomala	6852	9949	22.09.2023 18:39	Description	Download
guillaume	6851	9948	22.09.2023 10:20	Description	Download
laurandzis	6850	9947	22.09.2023 00:34	Description	Download
leonan0	6849	9946	21.09.2023 21:00	Description	Download
jennpowell617	6848	9944	21.09.2023 04:35	Description	Download
heuristiclynx	6847	9937	19.09.2023 13:55	Description	Download
jtmarder	6846	9934	18.09.2023 23:17	Description	Download
veda foxtrot	6845	9933	18.09.2023 19:05	Description	Download
hjwil132	6844	9932	18.09.2023 17:56	Description	Download
Wingidthing	6843	9930	17.09.2023 06:48	Description	Download
krystalpromise	6842	9929	17.09.2023 05:49	Description	Download
claire	6841	9928	17.09.2023 00:56	Description	Download
rokie6882	6840	9927	16.09.2023 16:32	Description	Download
etp51	6839	9923	14.09.2023 00:26	Description	Download
hablo	6838	9922	13.09.2023 17:41	Description	Download
30r3l365	6837	9921	13.09.2023 11:56	Description	Download

Show All Genotypes

Phenotypes

Name	Variations	# of Users
Skin color	White	1
Cutis Marmorata	Marmorata	1
blood type o+, RhD-	O+,rhd-	1
Palinopsia	Yes	1
Performance IQ(PIQ)	121	1
Can you make a rumbling noise occur inside your ears voluntarily? (Voluntary tensor tympani control)	Yes	2
jewish	Israeli sephardic	1
Hair brown eyes brown a+	Caucasian	1
Educational Attainment (2013)	A.s	2
Mood disorders	Bipolar ii disorder, substance/medication-induced bipolar disorder Major depressive disorder	2
Epicanthic Fold, Hooded Eyes	Double eyelid Epicanthic fold, not hooded eyelid	2
Cold-Induced Sweating	Yes	1
Emotional sweating (apocrine sweat glands)	High	1
Excessive sweating from heat (Eccrine sweat glands)	Yes No	3
Thin Skin	Skin	1
Difficulty reaching climax/ orgasming with partner	Almost impossible	2
Congenital adrenal hyperplasia (CAH)	Suspected diagnosis	1
Root resorption of tooth	Yes	1
Short Stature	Rs7659854(t;c)	1
Dementia Resistance	Rs11138902(g;a)	1

Show All Phenotypes

SNP comments

Comment by	Subject	Date	SNP
Deleted User	rs10513789(G/T) decreases the risk based on SNPedia but OPEN SNP says otherwise citing SNPedia!	25.04.2023 02:22	rs10513789
Lgarvey70458	T;C variation	10.12.2022 05:01	rs3
Ali	Marfan	18.11.2022 09:48	rs112989722
silverentei	C/G for Von Hippel-Lindau Syndrome - Ancestry miscall, or real?	29.06.2022 13:07	rs730882032
ShellSharked@gmail.com	Pathogenic - Dopamine Beta-Hydroxylase Deficiency	16.05.2022 00:16	rs74853476
Ali	Possible EDS	17.02.2022 10:53	rs1150753
katarina22	HLA-DQ2.2 Component	12.08.2021 21:01	rs7775228
jasonkotenko	This looks like a mis-classification	30.05.2021 22:31	rs485
hoghead352	Am I the lone A/A for rs369083786 or miscall?	13.11.2020 01:25	rs369083786
23andmere	-	18.06.2020 20:28	rs8050136
23andmere	-	18.06.2020 20:14	rs7903146
23andmere	-	18.06.2020 20:13	rs9939609
Deleted User	No matching genotype	30.05.2020 03:59	rs6265
Deleted User	-	30.05.2020 03:48	rs9939609
Deleted User	A/T	30.05.2020 03:39	rs9939609
Denatonium	-	10.04.2020 16:53	rs72921001
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

Phenotypes comments

Comment by	Phenotype	Subject	Date
Margalit	Ability to Tan	melanoma shouldn't be an either or for tanning.	10.08.2022 19:49
Alexander Richards	Nationality	-	16.02.2022 09:45
Denatonium	Covid19 Symptoms	-	22.03.2021 22:33
Alexander Richards	Gender	Biological sex and gender are also two different things.	09.02.2021 22:23
Alexander Richards	Gender	Try again	09.02.2021 22:22
JRD	Congenital Sucrase-Isomaltase Deficiency	-	03.08.2020 00:10
JRD	Congenital Sucrase-Isomaltase Deficiency	Made a mistake	03.08.2020 00:05
Jenifer	Do you have a parent who was diagnosed with Alzheimer's disease?	Parent and Alzheimer's	08.03.2020 20:24
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
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

Updates

New Publication

Users

New genotypes

Phenotypes

SNP comments

Phenotypes comments

Contacts