rs397516702

Orientation

plus

Stabilized

plus

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

Make rs397516702(G;T)

Make rs397516702(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31519873

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs397516702
dbSNP (classic)	rs397516702
ClinGen	rs397516702
ebi	rs397516702
HLI	rs397516702
Exac	rs397516702
Gnomad	rs397516702
Varsome	rs397516702
LitVar	rs397516702
Map	rs397516702
PheGenI	rs397516702
Biobank	rs397516702
1000 genomes	rs397516702
hgdp	rs397516702
ensembl	rs397516702
geneview	rs397516702
scholar	rs397516702
google	rs397516702
pharmgkb	rs397516702
gwascentral	rs397516702
openSNP	rs397516702
23andMe	rs397516702
SNPshot	rs397516702
SNPdbe	rs397516702
MSV3d	rs397516702
GWAS Ctlg	rs397516702

Max Magnitude

0

ClinVar
Risk	rs397516702(C;C) rs397516702(T;T)
Alt	rs397516702(C;C) rs397516702(T;T)
Reference	Rs397516702(G;G)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	DSG2
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000018.9:g.29099836G>C; NC_000018.9:g.29099836G>T
CLNSRC
CLNACC	RCV000181199.1, RCV000037266.3,