rs751012696

Orientation

plus

Stabilized

plus

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

Make rs751012696(A;A)

Make rs751012696(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31524763

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs751012696
dbSNP (classic)	rs751012696
ClinGen	rs751012696
ebi	rs751012696
HLI	rs751012696
Exac	rs751012696
Gnomad	rs751012696
Varsome	rs751012696
LitVar	rs751012696
Map	rs751012696
PheGenI	rs751012696
Biobank	rs751012696
1000 genomes	rs751012696
hgdp	rs751012696
ensembl	rs751012696
geneview	rs751012696
scholar	rs751012696
google	rs751012696
pharmgkb	rs751012696
gwascentral	rs751012696
openSNP	rs751012696
23andMe	rs751012696
SNPshot	rs751012696
SNPdbe	rs751012696
MSV3d	rs751012696
GWAS Ctlg	rs751012696

Max Magnitude

0

ClinVar
Risk	rs751012696(A;A)
Alt	rs751012696(A;A)
Reference	Rs751012696(G;G)
Significance	Pathogenic
Disease	not specified
Variation	info
Gene	DSG2
CLNDBN	not specified
Reversed	0
HGVS	NC_000018.9:g.29104726G>A
CLNSRC
CLNACC	RCV000181212.2,