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rs1064795631

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome11
Position2167474
GeneTH
is asnp
is mentioned by
dbSNPrs1064795631
dbSNP (old)rs1064795631
ClinGenrs1064795631
ebirs1064795631
HLIrs1064795631
Exacrs1064795631
Gnomadrs1064795631
Varsomers1064795631
Maprs1064795631
PheGenIrs1064795631
Biobankrs1064795631
1000 genomesrs1064795631
hgdprs1064795631
ensemblrs1064795631
gopubmedrs1064795631
geneviewrs1064795631
scholarrs1064795631
googlers1064795631
pharmgkbrs1064795631
gwascentralrs1064795631
openSNPrs1064795631
23andMers1064795631
23andMe allrs1064795631
SNPshotrs1064795631
SNPdbers1064795631
MSV3drs1064795631
GWAS Ctlgrs1064795631
Max Magnitude0
ClinVar
Risk rs1064795631(C;C)
Alt rs1064795631(C;C)
Reference Rs1064795631(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TH
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.2188704A>G
CLNSRC
CLNACC RCV000478105.1,