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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
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