Have questions? Visit https://www.reddit.com/r/SNPedia

rs472913

From SNPedia

Orientationplus
Stabilizedplus
Make rs472913(C;C)
Make rs472913(C;G)
Make rs472913(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position60629886
is asnp
is mentioned by
dbSNPrs472913
ebirs472913
HLIrs472913
Exacrs472913
Varsomers472913
Maprs472913
PheGenIrs472913
hapmaprs472913
1000 genomesrs472913
hgdprs472913
ensemblrs472913
gopubmedrs472913
geneviewrs472913
scholarrs472913
googlers472913
pharmgkbrs472913
gwascentralrs472913
openSNPrs472913
23andMers472913
23andMe allrs472913
SNP Nexus

SNPshotrs472913
SNPdbers472913
MSV3drs472913
GWAS Ctlgrs472913
GMAF0.4972
Max Magnitude
? (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]


GET Evidence
rs472913
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.4375
summary