rs587782933

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs587782933(A;A)

Make rs587782933(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

2504526

Gene

CACNA1C

is a	snp
is	mentioned by
dbSNP	rs587782933
dbSNP (classic)	rs587782933
ClinGen	rs587782933
ebi	rs587782933
HLI	rs587782933
Exac	rs587782933
Gnomad	rs587782933
Varsome	rs587782933
LitVar	rs587782933
Map	rs587782933
PheGenI	rs587782933
Biobank	rs587782933
1000 genomes	rs587782933
hgdp	rs587782933
ensembl	rs587782933
geneview	rs587782933
scholar	rs587782933
google	rs587782933
pharmgkb	rs587782933
gwascentral	rs587782933
openSNP	rs587782933
23andMe	rs587782933
SNPshot	rs587782933
SNPdbe	rs587782933
MSV3d	rs587782933
GWAS Ctlg	rs587782933

Max Magnitude

0

ClinVar
Risk	rs587782933(A;A)
Alt	rs587782933(A;A)
Reference	Rs587782933(G;G)
Significance	Pathogenic
Disease	Paroxysmal familial ventricular fibrillation 1 not provided
Variation	info
Gene	CACNA1C
CLNDBN	Paroxysmal familial ventricular fibrillation 1 not provided
Reversed	0
HGVS	NC_000012.11:g.2613692G>A
CLNSRC
CLNACC	RCV000143870.1, RCV000170768.5,