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rs1064793781

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position47806499
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs1064793781
dbSNP (old)rs1064793781
ClinGenrs1064793781
ebirs1064793781
HLIrs1064793781
Exacrs1064793781
Gnomadrs1064793781
Varsomers1064793781
Maprs1064793781
PheGenIrs1064793781
Biobankrs1064793781
1000 genomesrs1064793781
hgdprs1064793781
ensemblrs1064793781
gopubmedrs1064793781
geneviewrs1064793781
scholarrs1064793781
googlers1064793781
pharmgkbrs1064793781
gwascentralrs1064793781
openSNPrs1064793781
23andMers1064793781
23andMe allrs1064793781
SNPshotrs1064793781
SNPdbers1064793781
MSV3drs1064793781
GWAS Ctlgrs1064793781
Max Magnitude0
ClinVar
Risk rs1064793781(-;-)
Alt rs1064793781(-;-)
Reference Rs1064793781(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FBXO11 MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48033638delT
CLNSRC
CLNACC RCV000478924.1,