rs397517008

Orientation

minus

Stabilized

minus

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

Make rs397517008(-;-)

Make rs397517008(-;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

32824092

Gene

PKP2

is a	snp
is	mentioned by
dbSNP	rs397517008
dbSNP (classic)	rs397517008
ClinGen	rs397517008
ebi	rs397517008
HLI	rs397517008
Exac	rs397517008
Gnomad	rs397517008
Varsome	rs397517008
LitVar	rs397517008
Map	rs397517008
PheGenI	rs397517008
Biobank	rs397517008
1000 genomes	rs397517008
hgdp	rs397517008
ensembl	rs397517008
geneview	rs397517008
scholar	rs397517008
google	rs397517008
pharmgkb	rs397517008
gwascentral	rs397517008
openSNP	rs397517008
23andMe	rs397517008
SNPshot	rs397517008
SNPdbe	rs397517008
MSV3d	rs397517008
GWAS Ctlg	rs397517008

Max Magnitude

0

ClinVar
Risk	rs397517008(-;-)
Alt	rs397517008(-;-)
Reference	Rs397517008(G;G)
Significance	Probable-Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	PKP2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy
Reversed	1
HGVS	NC_000012.11:g.32977026delC
CLNSRC	ClinVar
CLNACC	RCV000038185.2,