rs397517393

Orientation

minus

Stabilized

minus

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

Make rs397517393(A;A)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31093558

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs397517393
dbSNP (classic)	rs397517393
ClinGen	rs397517393
ebi	rs397517393
HLI	rs397517393
Exac	rs397517393
Gnomad	rs397517393
Varsome	rs397517393
LitVar	rs397517393
Map	rs397517393
PheGenI	rs397517393
Biobank	rs397517393
1000 genomes	rs397517393
hgdp	rs397517393
ensembl	rs397517393
geneview	rs397517393
scholar	rs397517393
google	rs397517393
pharmgkb	rs397517393
gwascentral	rs397517393
openSNP	rs397517393
23andMe	rs397517393
SNPshot	rs397517393
SNPdbe	rs397517393
MSV3d	rs397517393
GWAS Ctlg	rs397517393

Max Magnitude

6.7

ClinVar
Risk	rs397517393(A;A)
Alt	rs397517393(A;A)
Reference	Rs397517393(G;G)
Significance	Probable-Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	DSC2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy
Reversed	1
HGVS	NC_000018.9:g.28673521C>T
CLNSRC	ClinVar
CLNACC	RCV000039409.2,