rs186906598

Orientation

plus

Stabilized

plus

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

Make rs186906598(A;A)

Make rs186906598(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

237627977

Gene

RYR2

is a	snp
is	mentioned by
dbSNP	rs186906598
dbSNP (classic)	rs186906598
ClinGen	rs186906598
ebi	rs186906598
HLI	rs186906598
Exac	rs186906598
Gnomad	rs186906598
Varsome	rs186906598
LitVar	rs186906598
Map	rs186906598
PheGenI	rs186906598
Biobank	rs186906598
1000 genomes	rs186906598
hgdp	rs186906598
ensembl	rs186906598
geneview	rs186906598
scholar	rs186906598
google	rs186906598
pharmgkb	rs186906598
gwascentral	rs186906598
openSNP	rs186906598
23andMe	rs186906598
SNPshot	rs186906598
SNPdbe	rs186906598
MSV3d	rs186906598
GWAS Ctlg	rs186906598

Max Magnitude

0

ClinVar
Risk	rs186906598(A;A)
Alt	rs186906598(A;A)
Reference	Rs186906598(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Ventricular tachycardia Catecholaminergic polymorphic ventricular tachycardia
Variation	info
Gene	RYR2
CLNDBN	not specified Ventricular tachycardia, catecholaminergic polymorphic, 1 Catecholaminergic polymorphic ventricular tachycardia
Reversed	0
HGVS	NC_000001.10:g.237791277G>A
CLNSRC
CLNACC	RCV000036777.5, RCV000171764.2, RCV000457463.1,