rs571985775

Orientation

plus

Stabilized

plus

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

Make rs571985775(A;A)

Make rs571985775(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

237785999

Gene

RYR2

is a	snp
is	mentioned by
dbSNP	rs571985775
dbSNP (classic)	rs571985775
ClinGen	rs571985775
ebi	rs571985775
HLI	rs571985775
Exac	rs571985775
Gnomad	rs571985775
Varsome	rs571985775
LitVar	rs571985775
Map	rs571985775
PheGenI	rs571985775
Biobank	rs571985775
1000 genomes	rs571985775
hgdp	rs571985775
ensembl	rs571985775
geneview	rs571985775
scholar	rs571985775
google	rs571985775
pharmgkb	rs571985775
gwascentral	rs571985775
openSNP	rs571985775
23andMe	rs571985775
SNPshot	rs571985775
SNPdbe	rs571985775
MSV3d	rs571985775
GWAS Ctlg	rs571985775

Max Magnitude

0

ClinVar
Risk	rs571985775(A;A)
Alt	rs571985775(A;A)
Reference	Rs571985775(G;G)
Significance	Pathogenic
Disease	not specified Catecholaminergic polymorphic ventricular tachycardia
Variation	info
Gene	RYR2
CLNDBN	not specified Catecholaminergic polymorphic ventricular tachycardia
Reversed	0
HGVS	NC_000001.10:g.237949299G>A
CLNSRC
CLNACC	RCV000151775.5, RCV000458521.1,