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rs587782933

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782933(A;A)
Make rs587782933(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position2504526
GeneCACNA1C
is asnp
is mentioned by
dbSNPrs587782933
ebirs587782933
HLIrs587782933
Exacrs587782933
Varsomers587782933
Maprs587782933
PheGenIrs587782933
hapmaprs587782933
1000 genomesrs587782933
hgdprs587782933
ensemblrs587782933
gopubmedrs587782933
geneviewrs587782933
scholarrs587782933
googlers587782933
pharmgkbrs587782933
gwascentralrs587782933
openSNPrs587782933
23andMers587782933
23andMe allrs587782933
SNP Nexus

SNPshotrs587782933
SNPdbers587782933
MSV3drs587782933
GWAS Ctlgrs587782933
Max Magnitude0
ClinVar
Risk rs587782933(A;A)
Alt rs587782933(A;A)
Reference rs587782933(G;G)
Significance Pathogenic
Disease VENTRICULAR FIBRILLATION not provided
Variation info
Gene CACNA1C
CLNDBN VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL not provided
Reversed 0
HGVS NC_000012.11:g.2613692G>A
CLNSRC
CLNACC RCV000143870.1, RCV000170768.3,