rs886039816

Orientation

minus

Stabilized

minus

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

Make rs886039816(A;G)

Make rs886039816(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

115732968

Gene

CASQ2

is a	snp
is	mentioned by
dbSNP	rs886039816
dbSNP (classic)	rs886039816
ClinGen	rs886039816
ebi	rs886039816
HLI	rs886039816
Exac	rs886039816
Gnomad	rs886039816
Varsome	rs886039816
LitVar	rs886039816
Map	rs886039816
PheGenI	rs886039816
Biobank	rs886039816
1000 genomes	rs886039816
hgdp	rs886039816
ensembl	rs886039816
geneview	rs886039816
scholar	rs886039816
google	rs886039816
pharmgkb	rs886039816
gwascentral	rs886039816
openSNP	rs886039816
23andMe	rs886039816
SNPshot	rs886039816
SNPdbe	rs886039816
MSV3d	rs886039816
GWAS Ctlg	rs886039816

Max Magnitude

0

ClinVar
Risk	rs886039816(G;G)
Alt	rs886039816(G;G)
Reference	Rs886039816(A;A)
Significance	Pathogenic
Disease	Ventricular tachycardia
Variation	info
Gene	CASQ2
CLNDBN	Ventricular tachycardia, catecholaminergic polymorphic, 2
Reversed	1
HGVS	NC_000001.10:g.116275589T>C
CLNSRC
CLNACC	RCV000256223.1,