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rs1064794055

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Chromosome2
Position47800011
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064794055
dbSNP (old)rs1064794055
ClinGenrs1064794055
ebirs1064794055
HLIrs1064794055
Exacrs1064794055
Gnomadrs1064794055
Varsomers1064794055
Maprs1064794055
PheGenIrs1064794055
Biobankrs1064794055
1000 genomesrs1064794055
hgdprs1064794055
ensemblrs1064794055
gopubmedrs1064794055
geneviewrs1064794055
scholarrs1064794055
googlers1064794055
pharmgkbrs1064794055
gwascentralrs1064794055
openSNPrs1064794055
23andMers1064794055
23andMe allrs1064794055
SNPshotrs1064794055
SNPdbers1064794055
MSV3drs1064794055
GWAS Ctlgrs1064794055
Max Magnitude0
ClinVar
Risk rs1064794055(-;-)
Alt rs1064794055(-;-)
Reference Rs1064794055(AA;AA)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48027150_48027151delAA
CLNSRC
CLNACC RCV000480920.1,