rs121918597

Orientation

plus

Stabilized

plus

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

Make rs121918597(C;T)

Make rs121918597(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

237634937

Gene

RYR2

is a	snp
is	mentioned by
dbSNP	rs121918597
dbSNP (classic)	rs121918597
ClinGen	rs121918597
ebi	rs121918597
HLI	rs121918597
Exac	rs121918597
Gnomad	rs121918597
Varsome	rs121918597
LitVar	rs121918597
Map	rs121918597
PheGenI	rs121918597
Biobank	rs121918597
1000 genomes	rs121918597
hgdp	rs121918597
ensembl	rs121918597
geneview	rs121918597
scholar	rs121918597
google	rs121918597
pharmgkb	rs121918597
gwascentral	rs121918597
openSNP	rs121918597
23andMe	rs121918597
SNPshot	rs121918597
SNPdbe	rs121918597
MSV3d	rs121918597
GWAS Ctlg	rs121918597

Max Magnitude

0

OMIM	180902
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121918597(T;T)
Alt	rs121918597(T;T)
Reference	Rs121918597(C;C)
Significance	Pathogenic
Disease	Ventricular tachycardia not provided Catecholaminergic polymorphic ventricular tachycardia
Variation	info
Gene	RYR2
CLNDBN	Ventricular tachycardia, catecholaminergic polymorphic, 1 not provided Catecholaminergic polymorphic ventricular tachycardia
Reversed	0
HGVS	NC_000001.10:g.237798237C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013820.17, RCV000182746.3, RCV000466223.1,