rs145476705

Orientation

plus

Stabilized

plus

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

Make rs145476705(A;T)

Make rs145476705(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

18

Position

31087781

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs145476705
dbSNP (classic)	rs145476705
ClinGen	rs145476705
ebi	rs145476705
HLI	rs145476705
Exac	rs145476705
Gnomad	rs145476705
Varsome	rs145476705
LitVar	rs145476705
Map	rs145476705
PheGenI	rs145476705
Biobank	rs145476705
1000 genomes	rs145476705
hgdp	rs145476705
ensembl	rs145476705
geneview	rs145476705
scholar	rs145476705
google	rs145476705
pharmgkb	rs145476705
gwascentral	rs145476705
openSNP	rs145476705
23andMe	rs145476705
SNPshot	rs145476705
SNPdbe	rs145476705
MSV3d	rs145476705
GWAS Ctlg	rs145476705

Max Magnitude

0

ClinVar
Risk	rs145476705(G;G) rs145476705(T;T)
Alt	rs145476705(G;G) rs145476705(T;T)
Reference	Rs145476705(A;A)
Significance	Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy not provided Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	DSC2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy not provided Arrhythmogenic right ventricular cardiomyopathy, type 11
Reversed	0
HGVS	NC_000018.9:g.28667744A>T
CLNSRC
CLNACC	RCV000149890.2, RCV000181141.1, RCV000458517.1,