rs576404380

Orientation

plus

Stabilized

plus

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

Make rs576404380(A;G)

Make rs576404380(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

18

Position

31535365

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs576404380
dbSNP (classic)	rs576404380
ClinGen	rs576404380
ebi	rs576404380
HLI	rs576404380
Exac	rs576404380
Gnomad	rs576404380
Varsome	rs576404380
LitVar	rs576404380
Map	rs576404380
PheGenI	rs576404380
Biobank	rs576404380
1000 genomes	rs576404380
hgdp	rs576404380
ensembl	rs576404380
geneview	rs576404380
scholar	rs576404380
google	rs576404380
pharmgkb	rs576404380
gwascentral	rs576404380
openSNP	rs576404380
23andMe	rs576404380
SNPshot	rs576404380
SNPdbe	rs576404380
MSV3d	rs576404380
GWAS Ctlg	rs576404380

Max Magnitude

0

ClinVar
Risk	rs576404380(G;G)
Alt	rs576404380(G;G)
Reference	Rs576404380(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DSG2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.29115328A>G
CLNSRC
CLNACC	RCV000171268.1,