rs587782975

Orientation

plus

Stabilized

plus

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

Make rs587782975(A;G)

Make rs587782975(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

237772024

Gene

RYR2

is a	snp
is	mentioned by
dbSNP	rs587782975
dbSNP (classic)	rs587782975
ClinGen	rs587782975
ebi	rs587782975
HLI	rs587782975
Exac	rs587782975
Gnomad	rs587782975
Varsome	rs587782975
LitVar	rs587782975
Map	rs587782975
PheGenI	rs587782975
Biobank	rs587782975
1000 genomes	rs587782975
hgdp	rs587782975
ensembl	rs587782975
geneview	rs587782975
scholar	rs587782975
google	rs587782975
pharmgkb	rs587782975
gwascentral	rs587782975
openSNP	rs587782975
23andMe	rs587782975
SNPshot	rs587782975
SNPdbe	rs587782975
MSV3d	rs587782975
GWAS Ctlg	rs587782975

Max Magnitude

0

ClinVar
Risk	rs587782975(G;G)
Alt	rs587782975(G;G)
Reference	Rs587782975(A;A)
Significance	Probable-Pathogenic
Disease	Ventricular tachycardia not specified
Variation	info
Gene	RYR2
CLNDBN	Ventricular tachycardia, catecholaminergic polymorphic, 1 not specified
Reversed	0
HGVS	NC_000001.10:g.237935324A>G
CLNSRC
CLNACC	RCV000143948.1, RCV000182797.3,