rs786205273

Orientation

plus

Stabilized

plus

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

Make rs786205273(-;G)

Make rs786205273(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

237614785

Gene

RYR2

is a	snp
is	mentioned by
dbSNP	rs786205273
dbSNP (classic)	rs786205273
ClinGen	rs786205273
ebi	rs786205273
HLI	rs786205273
Exac	rs786205273
Gnomad	rs786205273
Varsome	rs786205273
LitVar	rs786205273
Map	rs786205273
PheGenI	rs786205273
Biobank	rs786205273
1000 genomes	rs786205273
hgdp	rs786205273
ensembl	rs786205273
geneview	rs786205273
scholar	rs786205273
google	rs786205273
pharmgkb	rs786205273
gwascentral	rs786205273
openSNP	rs786205273
23andMe	rs786205273
SNPshot	rs786205273
SNPdbe	rs786205273
MSV3d	rs786205273
GWAS Ctlg	rs786205273

Max Magnitude

0

ClinVar
Risk	rs786205273(G;G)
Alt	rs786205273(G;G)
Reference	Rs786205273(-;-)
Significance	Probable-Pathogenic
Disease	Ventricular tachycardia
Variation	info
Gene	RYR2
CLNDBN	Ventricular tachycardia, polymorphic
Reversed	0
HGVS	NC_000001.10:g.237778085dupG
CLNSRC
CLNACC	RCV000171566.1,