rs794728094

Orientation

plus

Stabilized

plus

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

Make rs794728094(-;-)

Make rs794728094(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31530987

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs794728094
dbSNP (classic)	rs794728094
ClinGen	rs794728094
ebi	rs794728094
HLI	rs794728094
Exac	rs794728094
Gnomad	rs794728094
Varsome	rs794728094
LitVar	rs794728094
Map	rs794728094
PheGenI	rs794728094
Biobank	rs794728094
1000 genomes	rs794728094
hgdp	rs794728094
ensembl	rs794728094
geneview	rs794728094
scholar	rs794728094
google	rs794728094
pharmgkb	rs794728094
gwascentral	rs794728094
openSNP	rs794728094
23andMe	rs794728094
SNPshot	rs794728094
SNPdbe	rs794728094
MSV3d	rs794728094
GWAS Ctlg	rs794728094

Max Magnitude

0

ClinVar
Risk	rs794728094(-;-)
Alt	rs794728094(-;-)
Reference	Rs794728094(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DSG2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.29110950delG
CLNSRC
CLNACC	RCV000181241.2,