rs794728072

Orientation

minus

Stabilized

minus

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

Make rs794728072(-;-)

Make rs794728072(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31071604

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs794728072
dbSNP (classic)	rs794728072
ClinGen	rs794728072
ebi	rs794728072
HLI	rs794728072
Exac	rs794728072
Gnomad	rs794728072
Varsome	rs794728072
LitVar	rs794728072
Map	rs794728072
PheGenI	rs794728072
Biobank	rs794728072
1000 genomes	rs794728072
hgdp	rs794728072
ensembl	rs794728072
geneview	rs794728072
scholar	rs794728072
google	rs794728072
pharmgkb	rs794728072
gwascentral	rs794728072
openSNP	rs794728072
23andMe	rs794728072
SNPshot	rs794728072
SNPdbe	rs794728072
MSV3d	rs794728072
GWAS Ctlg	rs794728072

Max Magnitude

0

ClinVar
Risk	rs794728072(-;-)
Alt	rs794728072(-;-)
Reference	Rs794728072(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DSC2
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.28651570delC
CLNSRC
CLNACC	RCV000181172.2,