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rs1064793731

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome18
Position31070724
GeneDSC2
is asnp
is mentioned by
dbSNPrs1064793731
dbSNP (old)rs1064793731
ClinGenrs1064793731
ebirs1064793731
HLIrs1064793731
Exacrs1064793731
Gnomadrs1064793731
Varsomers1064793731
LitVarrs1064793731
Maprs1064793731
PheGenIrs1064793731
Biobankrs1064793731
1000 genomesrs1064793731
hgdprs1064793731
ensemblrs1064793731
gopubmedrs1064793731
geneviewrs1064793731
scholarrs1064793731
googlers1064793731
pharmgkbrs1064793731
gwascentralrs1064793731
openSNPrs1064793731
23andMers1064793731
23andMe allrs1064793731
SNPshotrs1064793731
SNPdbers1064793731
MSV3drs1064793731
GWAS Ctlgrs1064793731
Max Magnitude0
ClinVar
Risk rs1064793731(C;C)
Alt rs1064793731(C;C)
Reference Rs1064793731(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene DSC2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.28650690A>G
CLNSRC
CLNACC RCV000484544.1,