rs763955301

Orientation

plus

Stabilized

plus

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

Make rs763955301(-;-)

Make rs763955301(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

115732961

Gene

CASQ2

is a	snp
is	mentioned by
dbSNP	rs763955301
dbSNP (classic)	rs763955301
ClinGen	rs763955301
ebi	rs763955301
HLI	rs763955301
Exac	rs763955301
Gnomad	rs763955301
Varsome	rs763955301
LitVar	rs763955301
Map	rs763955301
PheGenI	rs763955301
Biobank	rs763955301
1000 genomes	rs763955301
hgdp	rs763955301
ensembl	rs763955301
geneview	rs763955301
scholar	rs763955301
google	rs763955301
pharmgkb	rs763955301
gwascentral	rs763955301
openSNP	rs763955301
23andMe	rs763955301
SNPshot	rs763955301
SNPdbe	rs763955301
MSV3d	rs763955301
GWAS Ctlg	rs763955301

Max Magnitude

0

ClinVar
Risk	rs763955301(-;-)
Alt	rs763955301(-;-)
Reference	Rs763955301(A;A)
Significance	Probable-Pathogenic
Disease	Ventricular tachycardia
Variation	info
Gene	CASQ2
CLNDBN	Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed	0
HGVS	NC_000001.10:g.116275582delA
CLNSRC
CLNACC	RCV000208054.1,