rs397517013

Orientation

minus

Stabilized

minus

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

Make rs397517013(-;GAAG)

Make rs397517013(GAAG;GAAG)

Reference

GRCh38 38.1/141

Chromosome

12

Position

32822482

Gene

PKP2

is a	snp
is	mentioned by
dbSNP	rs397517013
dbSNP (classic)	rs397517013
ClinGen	rs397517013
ebi	rs397517013
HLI	rs397517013
Exac	rs397517013
Gnomad	rs397517013
Varsome	rs397517013
LitVar	rs397517013
Map	rs397517013
PheGenI	rs397517013
Biobank	rs397517013
1000 genomes	rs397517013
hgdp	rs397517013
ensembl	rs397517013
geneview	rs397517013
scholar	rs397517013
google	rs397517013
pharmgkb	rs397517013
gwascentral	rs397517013
openSNP	rs397517013
23andMe	rs397517013
SNPshot	rs397517013
SNPdbe	rs397517013
MSV3d	rs397517013
GWAS Ctlg	rs397517013

Max Magnitude

0

ClinVar
Risk	rs397517013(GAAG;GAAG)
Alt	rs397517013(GAAG;GAAG)
Reference	Rs397517013(-;-)
Significance	Probable-Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	PKP2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy
Reversed	1
HGVS	NC_000012.11:g.32975417_32975420dupCTTC
CLNSRC	ClinVar
CLNACC	RCV000038191.2,