rs794728073

Orientation

minus

Stabilized

minus

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

Make rs794728073(-;-)

Make rs794728073(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31068915

Gene

DSC2

is a	snp
is	mentioned by
dbSNP	rs794728073
dbSNP (classic)	rs794728073
ClinGen	rs794728073
ebi	rs794728073
HLI	rs794728073
Exac	rs794728073
Gnomad	rs794728073
Varsome	rs794728073
LitVar	rs794728073
Map	rs794728073
PheGenI	rs794728073
Biobank	rs794728073
1000 genomes	rs794728073
hgdp	rs794728073
ensembl	rs794728073
geneview	rs794728073
scholar	rs794728073
google	rs794728073
pharmgkb	rs794728073
gwascentral	rs794728073
openSNP	rs794728073
23andMe	rs794728073
SNPshot	rs794728073
SNPdbe	rs794728073
MSV3d	rs794728073
GWAS Ctlg	rs794728073

Max Magnitude

0

ClinVar
Risk	rs794728073(-;-)
Alt	rs794728073(-;-)
Reference	Rs794728073(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DSC2
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.28648881delA
CLNSRC
CLNACC	RCV000181174.1,