rs397516703

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TG)	6.7	Arrhythmogenic right ventricular dysplasia
(TG;TG)	0	common in clinvar

Make rs397516703(-;-)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31538872

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs397516703
dbSNP (classic)	rs397516703
ClinGen	rs397516703
ebi	rs397516703
HLI	rs397516703
Exac	rs397516703
Gnomad	rs397516703
Varsome	rs397516703
LitVar	rs397516703
Map	rs397516703
PheGenI	rs397516703
Biobank	rs397516703
1000 genomes	rs397516703
hgdp	rs397516703
ensembl	rs397516703
geneview	rs397516703
scholar	rs397516703
google	rs397516703
pharmgkb	rs397516703
gwascentral	rs397516703
openSNP	rs397516703
23andMe	rs397516703
SNPshot	rs397516703
SNPdbe	rs397516703
MSV3d	rs397516703
GWAS Ctlg	rs397516703

Max Magnitude

6.7

aka c.1771_1772delTG

ClinVar
Risk	rs397516703(-;-)
Alt	rs397516703(-;-)
Reference	Rs397516703(TG;TG)
Significance	Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy not provided
Variation	info
Gene	DSG2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy not provided
Reversed	0
HGVS	NC_000018.9:g.29118835_29118836delTG
CLNSRC	ClinVar
CLNACC	RCV000037271.3, RCV000181243.1,