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rs1064796861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position229787503
GeneTRIP12
is asnp
is mentioned by
dbSNPrs1064796861
dbSNP (old)rs1064796861
ClinGenrs1064796861
ebirs1064796861
HLIrs1064796861
Exacrs1064796861
Gnomadrs1064796861
Varsomers1064796861
Maprs1064796861
PheGenIrs1064796861
Biobankrs1064796861
1000 genomesrs1064796861
hgdprs1064796861
ensemblrs1064796861
gopubmedrs1064796861
geneviewrs1064796861
scholarrs1064796861
googlers1064796861
pharmgkbrs1064796861
gwascentralrs1064796861
openSNPrs1064796861
23andMers1064796861
23andMe allrs1064796861
SNPshotrs1064796861
SNPdbers1064796861
MSV3drs1064796861
GWAS Ctlgrs1064796861
Max Magnitude0
ClinVar
Risk rs1064796861(C;C)
Alt rs1064796861(C;C)
Reference Rs1064796861(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TRIP12
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.230652219A>G
CLNSRC
CLNACC RCV000482024.1,