rs397517001

Orientation

minus

Stabilized

minus

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

Make rs397517001(A;A)

Reference

GRCh38 38.1/141

Chromosome

12

Position

32841102

Gene

PKP2

is a	snp
is	mentioned by
dbSNP	rs397517001
dbSNP (classic)	rs397517001
ClinGen	rs397517001
ebi	rs397517001
HLI	rs397517001
Exac	rs397517001
Gnomad	rs397517001
Varsome	rs397517001
LitVar	rs397517001
Map	rs397517001
PheGenI	rs397517001
Biobank	rs397517001
1000 genomes	rs397517001
hgdp	rs397517001
ensembl	rs397517001
geneview	rs397517001
scholar	rs397517001
google	rs397517001
pharmgkb	rs397517001
gwascentral	rs397517001
openSNP	rs397517001
23andMe	rs397517001
SNPshot	rs397517001
SNPdbe	rs397517001
MSV3d	rs397517001
GWAS Ctlg	rs397517001

Max Magnitude

6.7

ClinVar
Risk	rs397517001(A;A)
Alt	rs397517001(A;A)
Reference	Rs397517001(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.32994036C>T
CLNSRC	ClinVar
CLNACC	RCV000038175.2,