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rs1064794709

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome18
Position31546341
GeneDSG2, DSG2-AS1
is asnp
is mentioned by
dbSNPrs1064794709
dbSNP (classic)rs1064794709
ClinGenrs1064794709
ebirs1064794709
HLIrs1064794709
Exacrs1064794709
Gnomadrs1064794709
Varsomers1064794709
LitVarrs1064794709
Maprs1064794709
PheGenIrs1064794709
Biobankrs1064794709
1000 genomesrs1064794709
hgdprs1064794709
ensemblrs1064794709
geneviewrs1064794709
scholarrs1064794709
googlers1064794709
pharmgkbrs1064794709
gwascentralrs1064794709
openSNPrs1064794709
23andMers1064794709
SNPshotrs1064794709
SNPdbers1064794709
MSV3drs1064794709
GWAS Ctlgrs1064794709
Max Magnitude0
ClinVar
Risk rs1064794709(-;-)
Alt rs1064794709(-;-)
Reference Rs1064794709(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSG2-AS1 DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29126304delT
CLNSRC
CLNACC RCV000485291.1,