rs372827156

Orientation

plus

Stabilized

plus

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

Make rs372827156(A;A)

Reference

GRCh38 38.1/141

Chromosome

12

Position

32850907

Gene

PKP2

is a	snp
is	mentioned by
dbSNP	rs372827156
dbSNP (classic)	rs372827156
ClinGen	rs372827156
ebi	rs372827156
HLI	rs372827156
Exac	rs372827156
Gnomad	rs372827156
Varsome	rs372827156
LitVar	rs372827156
Map	rs372827156
PheGenI	rs372827156
Biobank	rs372827156
1000 genomes	rs372827156
hgdp	rs372827156
ensembl	rs372827156
geneview	rs372827156
scholar	rs372827156
google	rs372827156
pharmgkb	rs372827156
gwascentral	rs372827156
openSNP	rs372827156
23andMe	rs372827156
SNPshot	rs372827156
SNPdbe	rs372827156
MSV3d	rs372827156
GWAS Ctlg	rs372827156

Max Magnitude

6.7

ClinVar
Risk	rs372827156(A;A)
Alt	rs372827156(A;A)
Reference	Rs372827156(G;G)
Significance	Other
Disease	Arrhythmogenic right ventricular cardiomyopathy not provided Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	PKP2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy not provided Arrhythmogenic right ventricular cardiomyopathy, type 9
Reversed	0
HGVS	NC_000012.11:g.33003841G>A
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000038155.4, RCV000183740.4, RCV000471559.1,