Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064795963

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome18
Position31091029
GeneDSC2
is asnp
is mentioned by
dbSNPrs1064795963
dbSNP (old)rs1064795963
ClinGenrs1064795963
ebirs1064795963
HLIrs1064795963
Exacrs1064795963
Gnomadrs1064795963
Varsomers1064795963
LitVarrs1064795963
Maprs1064795963
PheGenIrs1064795963
Biobankrs1064795963
1000 genomesrs1064795963
hgdprs1064795963
ensemblrs1064795963
gopubmedrs1064795963
geneviewrs1064795963
scholarrs1064795963
googlers1064795963
pharmgkbrs1064795963
gwascentralrs1064795963
openSNPrs1064795963
23andMers1064795963
23andMe allrs1064795963
SNPshotrs1064795963
SNPdbers1064795963
MSV3drs1064795963
GWAS Ctlgrs1064795963
Max Magnitude0
ClinVar
Risk rs1064795963(-;-)
Alt rs1064795963(-;-)
Reference Rs1064795963(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSC2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.28670992delT
CLNSRC
CLNACC RCV000482916.1,