rs727503396

Orientation

plus

Stabilized

plus

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

Make rs727503396(A;A)

Make rs727503396(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

237369589

Gene

RYR2

is a	snp
is	mentioned by
dbSNP	rs727503396
dbSNP (classic)	rs727503396
ClinGen	rs727503396
ebi	rs727503396
HLI	rs727503396
Exac	rs727503396
Gnomad	rs727503396
Varsome	rs727503396
LitVar	rs727503396
Map	rs727503396
PheGenI	rs727503396
Biobank	rs727503396
1000 genomes	rs727503396
hgdp	rs727503396
ensembl	rs727503396
geneview	rs727503396
scholar	rs727503396
google	rs727503396
pharmgkb	rs727503396
gwascentral	rs727503396
openSNP	rs727503396
23andMe	rs727503396
SNPshot	rs727503396
SNPdbe	rs727503396
MSV3d	rs727503396
GWAS Ctlg	rs727503396

Max Magnitude

0

ClinVar
Risk	rs727503396(A;A)
Alt	rs727503396(A;A)
Reference	Rs727503396(G;G)
Significance	Probable-Pathogenic
Disease	not specified Ventricular tachycardia
Variation	info
Gene	RYR2
CLNDBN	not specified Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed	0
HGVS	NC_000001.10:g.237532889G>A
CLNSRC
CLNACC	RCV000151753.1, RCV000157442.1,