rs794728083

Orientation

plus

Stabilized

plus

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

Make rs794728083(C;T)

Make rs794728083(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31524526

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs794728083
dbSNP (classic)	rs794728083
ClinGen	rs794728083
ebi	rs794728083
HLI	rs794728083
Exac	rs794728083
Gnomad	rs794728083
Varsome	rs794728083
LitVar	rs794728083
Map	rs794728083
PheGenI	rs794728083
Biobank	rs794728083
1000 genomes	rs794728083
hgdp	rs794728083
ensembl	rs794728083
geneview	rs794728083
scholar	rs794728083
google	rs794728083
pharmgkb	rs794728083
gwascentral	rs794728083
openSNP	rs794728083
23andMe	rs794728083
SNPshot	rs794728083
SNPdbe	rs794728083
MSV3d	rs794728083
GWAS Ctlg	rs794728083

Max Magnitude

0

ClinVar
Risk	rs794728083(T;T)
Alt	rs794728083(T;T)
Reference	Rs794728083(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DSG2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.29104489C>T
CLNSRC
CLNACC	RCV000181208.1,