rs397507555

Orientation

minus

Stabilized

minus

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

Make rs397507555(-;-)

Make rs397507555(-;A)

Reference

GRCh38 38.1/141

Chromosome

1

Position

115768480

Gene

CASQ2

is a	snp
is	mentioned by
dbSNP	rs397507555
dbSNP (classic)	rs397507555
ClinGen	rs397507555
ebi	rs397507555
HLI	rs397507555
Exac	rs397507555
Gnomad	rs397507555
Varsome	rs397507555
LitVar	rs397507555
Map	rs397507555
PheGenI	rs397507555
Biobank	rs397507555
1000 genomes	rs397507555
hgdp	rs397507555
ensembl	rs397507555
geneview	rs397507555
scholar	rs397507555
google	rs397507555
pharmgkb	rs397507555
gwascentral	rs397507555
openSNP	rs397507555
23andMe	rs397507555
SNPshot	rs397507555
SNPdbe	rs397507555
MSV3d	rs397507555
GWAS Ctlg	rs397507555

Max Magnitude

0

ClinVar
Risk	rs397507555(-;-)
Alt	rs397507555(-;-)
Reference	Rs397507555(A;A)
Significance	Pathogenic
Disease	Ventricular tachycardia
Variation	info
Gene	CASQ2
CLNDBN	Ventricular tachycardia, catecholaminergic polymorphic, 2
Reversed	1
HGVS	NC_000001.10:g.116311101delT
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000033941.2,