rs121913008

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6.7	Arrhythmogenic right ventricular dysplasia
(G;G)	0	common in clinvar

Make rs121913008(A;A)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31519858

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs121913008
dbSNP (classic)	rs121913008
ClinGen	rs121913008
ebi	rs121913008
HLI	rs121913008
Exac	rs121913008
Gnomad	rs121913008
Varsome	rs121913008
LitVar	rs121913008
Map	rs121913008
PheGenI	rs121913008
Biobank	rs121913008
1000 genomes	rs121913008
hgdp	rs121913008
ensembl	rs121913008
geneview	rs121913008
scholar	rs121913008
google	rs121913008
pharmgkb	rs121913008
gwascentral	rs121913008
openSNP	rs121913008
23andMe	rs121913008
SNPshot	rs121913008
SNPdbe	rs121913008
MSV3d	rs121913008
GWAS Ctlg	rs121913008

Max Magnitude

6.7

OMIM	125671
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121913008(A;A)
Alt	rs121913008(A;A)
Reference	Rs121913008(G;G)
Significance	Other
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.29099821G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018305.34, RCV000181197.3, RCV000211714.1,