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rs758282201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs758282201(-;-)
Make rs758282201(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position31519812
GeneDSG2
is asnp
is mentioned by
dbSNPrs758282201
dbSNP (classic)rs758282201
ClinGenrs758282201
ebirs758282201
HLIrs758282201
Exacrs758282201
Gnomadrs758282201
Varsomers758282201
LitVarrs758282201
Maprs758282201
PheGenIrs758282201
Biobankrs758282201
1000 genomesrs758282201
hgdprs758282201
ensemblrs758282201
geneviewrs758282201
scholarrs758282201
googlers758282201
pharmgkbrs758282201
gwascentralrs758282201
openSNPrs758282201
23andMers758282201
SNPshotrs758282201
SNPdbers758282201
MSV3drs758282201
GWAS Ctlgrs758282201
Max Magnitude0
ClinVar
Risk rs758282201(-;-)
Alt rs758282201(-;-)
Reference Rs758282201(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29099775delA
CLNSRC
CLNACC RCV000480668.1,