rs397517389

Orientation

minus

Stabilized

minus

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

Make rs397517389(G;G)

Make rs397517389(G;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31082924

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs397517389
dbSNP (classic)	rs397517389
ClinGen	rs397517389
ebi	rs397517389
HLI	rs397517389
Exac	rs397517389
Gnomad	rs397517389
Varsome	rs397517389
LitVar	rs397517389
Map	rs397517389
PheGenI	rs397517389
Biobank	rs397517389
1000 genomes	rs397517389
hgdp	rs397517389
ensembl	rs397517389
geneview	rs397517389
scholar	rs397517389
google	rs397517389
pharmgkb	rs397517389
gwascentral	rs397517389
openSNP	rs397517389
23andMe	rs397517389
SNPshot	rs397517389
SNPdbe	rs397517389
MSV3d	rs397517389
GWAS Ctlg	rs397517389

Max Magnitude

0

ClinVar
Risk	rs397517389(G;G)
Alt	rs397517389(G;G)
Reference	Rs397517389(T;T)
Significance	Probable-Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	DSC2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy
Reversed	1
HGVS	NC_000018.9:g.28662890A>C
CLNSRC	ClinVar
CLNACC	RCV000039401.2,