rs794728075

Orientation

minus

Stabilized

minus

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

Make rs794728075(C;G)

Make rs794728075(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31082378

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs794728075
dbSNP (classic)	rs794728075
ClinGen	rs794728075
ebi	rs794728075
HLI	rs794728075
Exac	rs794728075
Gnomad	rs794728075
Varsome	rs794728075
LitVar	rs794728075
Map	rs794728075
PheGenI	rs794728075
Biobank	rs794728075
1000 genomes	rs794728075
hgdp	rs794728075
ensembl	rs794728075
geneview	rs794728075
scholar	rs794728075
google	rs794728075
pharmgkb	rs794728075
gwascentral	rs794728075
openSNP	rs794728075
23andMe	rs794728075
SNPshot	rs794728075
SNPdbe	rs794728075
MSV3d	rs794728075
GWAS Ctlg	rs794728075

Max Magnitude

0

ClinVar
Risk	rs794728075(G;G) rs794728075(T;T)
Alt	rs794728075(G;G) rs794728075(T;T)
Reference	Rs794728075(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DSC2
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.28662344G>C
CLNSRC
CLNACC	RCV000181177.1,