rs397517015

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	6.7	Arrhythmogenic right ventricular dysplasia

Make rs397517015(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

32821502

Gene

PKP2

is a	snp
is	mentioned by
dbSNP	rs397517015
dbSNP (classic)	rs397517015
ClinGen	rs397517015
ebi	rs397517015
HLI	rs397517015
Exac	rs397517015
Gnomad	rs397517015
Varsome	rs397517015
LitVar	rs397517015
Map	rs397517015
PheGenI	rs397517015
Biobank	rs397517015
1000 genomes	rs397517015
hgdp	rs397517015
ensembl	rs397517015
geneview	rs397517015
scholar	rs397517015
google	rs397517015
pharmgkb	rs397517015
gwascentral	rs397517015
openSNP	rs397517015
23andMe	rs397517015
SNPshot	rs397517015
SNPdbe	rs397517015
MSV3d	rs397517015
GWAS Ctlg	rs397517015

Max Magnitude

6.7

ClinVar
Risk	rs397517015(T;T)
Alt	rs397517015(T;T)
Reference	Rs397517015(G;G)
Significance	Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	PKP2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy
Reversed	1
HGVS	NC_000012.11:g.32974436C>A
CLNSRC	ClinVar
CLNACC	RCV000038194.2,