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rs13409348

From SNPedia

Orientationplus
Stabilizedplus
Make rs13409348(C;C)
Make rs13409348(C;G)
Make rs13409348(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position79312862
is asnp
is mentioned by
dbSNPrs13409348
ebirs13409348
HLIrs13409348
Exacrs13409348
Varsomers13409348
Maprs13409348
PheGenIrs13409348
hapmaprs13409348
1000 genomesrs13409348
hgdprs13409348
ensemblrs13409348
gopubmedrs13409348
geneviewrs13409348
scholarrs13409348
googlers13409348
pharmgkbrs13409348
gwascentralrs13409348
openSNPrs13409348
23andMers13409348
23andMe allrs13409348
SNP Nexus

SNPshotrs13409348
SNPdbers13409348
MSV3drs13409348
GWAS Ctlgrs13409348
GMAF0.2626
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 G
P-val 0.000003
Odds Ratio 1.20 [1.11-1.29]


GET Evidence
rs13409348
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.328125
summary