rs397517003

Orientation

minus

Stabilized

minus

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

Make rs397517003(A;A)

Make rs397517003(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

32841027

Gene

PKP2

is a	snp
is	mentioned by
dbSNP	rs397517003
dbSNP (classic)	rs397517003
ClinGen	rs397517003
ebi	rs397517003
HLI	rs397517003
Exac	rs397517003
Gnomad	rs397517003
Varsome	rs397517003
LitVar	rs397517003
Map	rs397517003
PheGenI	rs397517003
Biobank	rs397517003
1000 genomes	rs397517003
hgdp	rs397517003
ensembl	rs397517003
geneview	rs397517003
scholar	rs397517003
google	rs397517003
pharmgkb	rs397517003
gwascentral	rs397517003
openSNP	rs397517003
23andMe	rs397517003
SNPshot	rs397517003
SNPdbe	rs397517003
MSV3d	rs397517003
GWAS Ctlg	rs397517003

Max Magnitude

0

ClinVar
Risk	rs397517003(A;A)
Alt	rs397517003(A;A)
Reference	Rs397517003(G;G)
Significance	Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy not provided
Variation	info
Gene	PKP2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy not provided
Reversed	1
HGVS	NC_000012.11:g.32993961C>T
CLNSRC	ClinVar
CLNACC	RCV000038177.2, RCV000183750.2,