rs794728093

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CTTGAAGGGATG;CTTGAAGGGATG)	0	common in clinvar
(GCTTGAAGGGAT;GCTTGAAGGGAT)	0	common in clinvar

Make rs794728093(-;-)

Make rs794728093(-;CTTGAAGGGATG)

Reference

GRCh38.p2 38.2/146

Chromosome

18

Position

31524703

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs794728093
dbSNP (classic)	rs794728093
ClinGen	rs794728093
ebi	rs794728093
HLI	rs794728093
Exac	rs794728093
Gnomad	rs794728093
Varsome	rs794728093
LitVar	rs794728093
Map	rs794728093
PheGenI	rs794728093
Biobank	rs794728093
1000 genomes	rs794728093
hgdp	rs794728093
ensembl	rs794728093
geneview	rs794728093
scholar	rs794728093
google	rs794728093
pharmgkb	rs794728093
gwascentral	rs794728093
openSNP	rs794728093
23andMe	rs794728093
SNPshot	rs794728093
SNPdbe	rs794728093
MSV3d	rs794728093
GWAS Ctlg	rs794728093

Max Magnitude

0

ClinVar
Risk	rs794728093(-;-) Rs794728093(GCTTGAAGGGAT;GCTTGAAGGGAT)
Alt	rs794728093(-;-) Rs794728093(GCTTGAAGGGAT;GCTTGAAGGGAT)
Reference	Rs794728093(CTTGAAGGGATG;CTTGAAGGGATG)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	DSG2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.29104666_29104677delCTTGAAGGGATG
CLNSRC
CLNACC	RCV000181240.2,