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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
Show All Genotypes
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
Show All Phenotypes
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