rs397517406

Orientation

minus

Stabilized

minus

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

Make rs397517406(C;G)

Make rs397517406(G;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31086672

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs397517406
dbSNP (classic)	rs397517406
ClinGen	rs397517406
ebi	rs397517406
HLI	rs397517406
Exac	rs397517406
Gnomad	rs397517406
Varsome	rs397517406
LitVar	rs397517406
Map	rs397517406
PheGenI	rs397517406
Biobank	rs397517406
1000 genomes	rs397517406
hgdp	rs397517406
ensembl	rs397517406
geneview	rs397517406
scholar	rs397517406
google	rs397517406
pharmgkb	rs397517406
gwascentral	rs397517406
openSNP	rs397517406
23andMe	rs397517406
SNPshot	rs397517406
SNPdbe	rs397517406
MSV3d	rs397517406
GWAS Ctlg	rs397517406

Max Magnitude

0

ClinVar
Risk	rs397517406(A;A) rs397517406(G;G)
Alt	rs397517406(A;A) rs397517406(G;G)
Reference	Rs397517406(C;C)
Significance	Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy not provided
Variation	info
Gene	DSC2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy not provided
Reversed	1
HGVS	NC_000018.9:g.28666635G>C
CLNSRC	ClinVar
CLNACC	RCV000039442.2, RCV000181144.2,