rs794728092

Orientation

plus

Stabilized

plus

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

Make rs794728092(-;-)

Make rs794728092(-;GTATC)

Make rs794728092(GTATC;GTATC)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31522160

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs794728092
dbSNP (classic)	rs794728092
ClinGen	rs794728092
ebi	rs794728092
HLI	rs794728092
Exac	rs794728092
Gnomad	rs794728092
Varsome	rs794728092
LitVar	rs794728092
Map	rs794728092
PheGenI	rs794728092
Biobank	rs794728092
1000 genomes	rs794728092
hgdp	rs794728092
ensembl	rs794728092
geneview	rs794728092
scholar	rs794728092
google	rs794728092
pharmgkb	rs794728092
gwascentral	rs794728092
openSNP	rs794728092
23andMe	rs794728092
SNPshot	rs794728092
SNPdbe	rs794728092
MSV3d	rs794728092
GWAS Ctlg	rs794728092

Max Magnitude

0

ClinVar
Risk	rs794728092(-;-)
Alt	rs794728092(-;-)
Reference	Rs794728092(ATCGT;ATCGT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DSG2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.29102123_29102127delGTATC
CLNSRC
CLNACC	RCV000181239.2,