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rs915071

From SNPedia

Orientationplus
Stabilizedplus
Make rs915071(C;C)
Make rs915071(C;T)
Make rs915071(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position31964652
is asnp
is mentioned by
dbSNPrs915071
dbSNP (classic)rs915071
ClinGenrs915071
ebirs915071
HLIrs915071
Exacrs915071
Gnomadrs915071
Varsomers915071
LitVarrs915071
Maprs915071
PheGenIrs915071
Biobankrs915071
1000 genomesrs915071
hgdprs915071
ensemblrs915071
geneviewrs915071
scholarrs915071
googlers915071
pharmgkbrs915071
gwascentralrs915071
openSNPrs915071
23andMers915071
SNPshotrs915071
SNPdbers915071
MSV3drs915071
GWAS Ctlgrs915071
GMAF0.3972
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 20889312]
Trait
Title A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder
Risk Allele A
P-val 0.000002
Odds Ratio 1.23 [NR]

[PMID 19571809OA-icon.png] Common variants on chromosome 6p22.1 are associated with schizophrenia.