rs373542380

Orientation

plus

Stabilized

plus

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

Make rs373542380(A;A)

Make rs373542380(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31521111

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs373542380
dbSNP (classic)	rs373542380
ClinGen	rs373542380
ebi	rs373542380
HLI	rs373542380
Exac	rs373542380
Gnomad	rs373542380
Varsome	rs373542380
LitVar	rs373542380
Map	rs373542380
PheGenI	rs373542380
Biobank	rs373542380
1000 genomes	rs373542380
hgdp	rs373542380
ensembl	rs373542380
geneview	rs373542380
scholar	rs373542380
google	rs373542380
pharmgkb	rs373542380
gwascentral	rs373542380
openSNP	rs373542380
23andMe	rs373542380
SNPshot	rs373542380
SNPdbe	rs373542380
MSV3d	rs373542380
GWAS Ctlg	rs373542380

Max Magnitude

0

ClinVar
Risk	rs373542380(A;A) rs373542380(T;T)
Alt	rs373542380(A;A) rs373542380(T;T)
Reference	Rs373542380(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	DSG2
CLNDBN	not specified
Reversed	0
HGVS	NC_000018.9:g.29101074G>A
CLNSRC
CLNACC	RCV000037304.3,