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rs472913

From SNPedia

Orientationplus
Stabilizedplus
Make rs472913(C;C)
Make rs472913(C;G)
Make rs472913(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position60629886
GeneLOC105378763
is asnp
is mentioned by
dbSNPrs472913
dbSNP (classic)rs472913
ClinGenrs472913
ebirs472913
HLIrs472913
Exacrs472913
Gnomadrs472913
Varsomers472913
LitVarrs472913
Maprs472913
PheGenIrs472913
Biobankrs472913
1000 genomesrs472913
hgdprs472913
ensemblrs472913
geneviewrs472913
scholarrs472913
googlers472913
pharmgkbrs472913
gwascentralrs472913
openSNPrs472913
23andMers472913
SNPshotrs472913
SNPdbers472913
MSV3drs472913
GWAS Ctlgrs472913
GMAF0.4972
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 19416921OA-icon.png]
Trait Bipolar disorder
Title Genome-wide association and meta-analysis of

bipolar disorder in individuals of European ancestry

Risk Allele C
P-val 2E-7
Odds Ratio 1.18 [1.11-1.25]