rs774863785

Orientation

plus

Stabilized

plus

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

Make rs774863785(A;A)

Make rs774863785(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31531167

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs774863785
dbSNP (classic)	rs774863785
ClinGen	rs774863785
ebi	rs774863785
HLI	rs774863785
Exac	rs774863785
Gnomad	rs774863785
Varsome	rs774863785
LitVar	rs774863785
Map	rs774863785
PheGenI	rs774863785
Biobank	rs774863785
1000 genomes	rs774863785
hgdp	rs774863785
ensembl	rs774863785
geneview	rs774863785
scholar	rs774863785
google	rs774863785
pharmgkb	rs774863785
gwascentral	rs774863785
openSNP	rs774863785
23andMe	rs774863785
SNPshot	rs774863785
SNPdbe	rs774863785
MSV3d	rs774863785
GWAS Ctlg	rs774863785

Max Magnitude

0

ClinVar
Risk	rs774863785(A;A)
Alt	rs774863785(A;A)
Reference	Rs774863785(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DSG2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.29111130G>A
CLNSRC
CLNACC	RCV000181216.2,