rs397514038

Orientation

plus

Stabilized

plus

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

Make rs397514038(A;G)

Make rs397514038(G;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31541191

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs397514038
dbSNP (classic)	rs397514038
ClinGen	rs397514038
ebi	rs397514038
HLI	rs397514038
Exac	rs397514038
Gnomad	rs397514038
Varsome	rs397514038
LitVar	rs397514038
Map	rs397514038
PheGenI	rs397514038
Biobank	rs397514038
1000 genomes	rs397514038
hgdp	rs397514038
ensembl	rs397514038
geneview	rs397514038
scholar	rs397514038
google	rs397514038
pharmgkb	rs397514038
gwascentral	rs397514038
openSNP	rs397514038
23andMe	rs397514038
SNPshot	rs397514038
SNPdbe	rs397514038
MSV3d	rs397514038
GWAS Ctlg	rs397514038

Max Magnitude

0

ClinVar
Risk	rs397514038(G;G)
Alt	rs397514038(G;G)
Reference	Rs397514038(A;A)
Significance	Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy not provided Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	DSG2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy, type 10 not provided Arrhythmogenic right ventricular cardiomyopathy
Reversed	0
HGVS	NC_000018.9:g.29121154A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018310.31, RCV000181225.1, RCV000211716.1,