rs121918604

Orientation

plus

Stabilized

plus

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

Make rs121918604(G;T)

Make rs121918604(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

237798037

Gene

RYR2

is a	snp
is	mentioned by
dbSNP	rs121918604
dbSNP (classic)	rs121918604
ClinGen	rs121918604
ebi	rs121918604
HLI	rs121918604
Exac	rs121918604
Gnomad	rs121918604
Varsome	rs121918604
LitVar	rs121918604
Map	rs121918604
PheGenI	rs121918604
Biobank	rs121918604
1000 genomes	rs121918604
hgdp	rs121918604
ensembl	rs121918604
geneview	rs121918604
scholar	rs121918604
google	rs121918604
pharmgkb	rs121918604
gwascentral	rs121918604
openSNP	rs121918604
23andMe	rs121918604
SNPshot	rs121918604
SNPdbe	rs121918604
MSV3d	rs121918604
GWAS Ctlg	rs121918604

Max Magnitude

0

OMIM	180902
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121918604(A;A) rs121918604(T;T)
Alt	rs121918604(A;A) rs121918604(T;T)
Reference	Rs121918604(G;G)
Significance	Other
Disease	Ventricular tachycardia
Variation	info
Gene	RYR2
CLNDBN	Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed	0
HGVS	NC_000001.10:g.237961337G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013827.25,