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rs41276445

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41276445(A;A)
Make rs41276445(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position53730470
GeneCACNA1D
is asnp
is mentioned by
dbSNPrs41276445
ebirs41276445
HLIrs41276445
Exacrs41276445
Varsomers41276445
Maprs41276445
PheGenIrs41276445
hapmaprs41276445
1000 genomesrs41276445
hgdprs41276445
ensemblrs41276445
gopubmedrs41276445
geneviewrs41276445
scholarrs41276445
googlers41276445
pharmgkbrs41276445
gwascentralrs41276445
openSNPrs41276445
23andMers41276445
23andMe allrs41276445
SNP Nexus

SNPshotrs41276445
SNPdbers41276445
MSV3drs41276445
GWAS Ctlgrs41276445
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs41276445(A,G,T;A,G,T)
Alt rs41276445(A,G,T;A,G,T)
Reference rs41276445(C;C)
Significance Pathogenic
Disease Primary aldosteronism not provided
Variation info
Gene CACNA1D
CLNDBN Primary aldosteronism, seizures, and neurologic abnormalities not provided
Reversed 0
HGVS NC_000003.11:g.53764497C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000056308.27, RCV000122488.1,