rs794728076

Orientation

minus

Stabilized

minus

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

Make rs794728076(A;A)

Make rs794728076(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31080340

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs794728076
dbSNP (classic)	rs794728076
ClinGen	rs794728076
ebi	rs794728076
HLI	rs794728076
Exac	rs794728076
Gnomad	rs794728076
Varsome	rs794728076
LitVar	rs794728076
Map	rs794728076
PheGenI	rs794728076
Biobank	rs794728076
1000 genomes	rs794728076
hgdp	rs794728076
ensembl	rs794728076
geneview	rs794728076
scholar	rs794728076
google	rs794728076
pharmgkb	rs794728076
gwascentral	rs794728076
openSNP	rs794728076
23andMe	rs794728076
SNPshot	rs794728076
SNPdbe	rs794728076
MSV3d	rs794728076
GWAS Ctlg	rs794728076

Max Magnitude

0

ClinVar
Risk	rs794728076(A;A)
Alt	rs794728076(A;A)
Reference	Rs794728076(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	DSC2
CLNDBN	not specified
Reversed	1
HGVS	NC_000018.9:g.28660306C>T
CLNSRC
CLNACC	RCV000181178.2,