rs397517395

Orientation

minus

Stabilized

minus

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

Make rs397517395(G;G)

Make rs397517395(G;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31071792

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs397517395
dbSNP (classic)	rs397517395
ClinGen	rs397517395
ebi	rs397517395
HLI	rs397517395
Exac	rs397517395
Gnomad	rs397517395
Varsome	rs397517395
LitVar	rs397517395
Map	rs397517395
PheGenI	rs397517395
Biobank	rs397517395
1000 genomes	rs397517395
hgdp	rs397517395
ensembl	rs397517395
geneview	rs397517395
scholar	rs397517395
google	rs397517395
pharmgkb	rs397517395
gwascentral	rs397517395
openSNP	rs397517395
23andMe	rs397517395
SNPshot	rs397517395
SNPdbe	rs397517395
MSV3d	rs397517395
GWAS Ctlg	rs397517395

Max Magnitude

0

ClinVar
Risk	rs397517395(C;C) rs397517395(G;G)
Alt	rs397517395(C;C) rs397517395(G;G)
Reference	Rs397517395(T;T)
Significance	Probable-Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy not specified
Variation	info
Gene	DSC2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy not specified
Reversed	1
HGVS	NC_000018.9:g.28651758A>C; NC_000018.9:g.28651758A>G
CLNSRC	ClinVar
CLNACC	RCV000039415.2, RCV000443484.1,