rs200804638

Orientation

plus

Stabilized

plus

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

Make rs200804638(C;T)

Make rs200804638(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31541198

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs200804638
dbSNP (classic)	rs200804638
ClinGen	rs200804638
ebi	rs200804638
HLI	rs200804638
Exac	rs200804638
Gnomad	rs200804638
Varsome	rs200804638
LitVar	rs200804638
Map	rs200804638
PheGenI	rs200804638
Biobank	rs200804638
1000 genomes	rs200804638
hgdp	rs200804638
ensembl	rs200804638
geneview	rs200804638
scholar	rs200804638
google	rs200804638
pharmgkb	rs200804638
gwascentral	rs200804638
openSNP	rs200804638
23andMe	rs200804638
SNPshot	rs200804638
SNPdbe	rs200804638
MSV3d	rs200804638
GWAS Ctlg	rs200804638

Max Magnitude

0

ClinVar
Risk	rs200804638(T;T)
Alt	rs200804638(T;T)
Reference	Rs200804638(C;C)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	DSG2
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000018.9:g.29121161C>T
CLNSRC
CLNACC	RCV000181226.1, RCV000223710.1,