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rs16966460

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16966460(C;G)
Make rs16966460(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position38219782
is asnp
is mentioned by
dbSNPrs16966460
ebirs16966460
HLIrs16966460
Exacrs16966460
Varsomers16966460
Maprs16966460
PheGenIrs16966460
hapmaprs16966460
1000 genomesrs16966460
hgdprs16966460
ensemblrs16966460
gopubmedrs16966460
geneviewrs16966460
scholarrs16966460
googlers16966460
pharmgkbrs16966460
gwascentralrs16966460
openSNPrs16966460
23andMers16966460
23andMe allrs16966460
SNP Nexus

SNPshotrs16966460
SNPdbers16966460
MSV3drs16966460
GWAS Ctlgrs16966460
GMAF0.1198
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 18711365OA-icon.png]
Trait Bipolar disorder
Title Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
Risk Allele G
P-val 0.0000039999999999999998
Odds Ratio 1.26 [NR]


GET Evidence
rs16966460
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary