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rs1064794302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position47801123
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064794302
dbSNP (old)rs1064794302
ClinGenrs1064794302
ebirs1064794302
HLIrs1064794302
Exacrs1064794302
Gnomadrs1064794302
Varsomers1064794302
Maprs1064794302
PheGenIrs1064794302
Biobankrs1064794302
1000 genomesrs1064794302
hgdprs1064794302
ensemblrs1064794302
gopubmedrs1064794302
geneviewrs1064794302
scholarrs1064794302
googlers1064794302
pharmgkbrs1064794302
gwascentralrs1064794302
openSNPrs1064794302
23andMers1064794302
23andMe allrs1064794302
SNPshotrs1064794302
SNPdbers1064794302
MSV3drs1064794302
GWAS Ctlgrs1064794302
Max Magnitude0
ClinVar
Risk rs1064794302(A;A)
Alt rs1064794302(A;A)
Reference Rs1064794302(G;G)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48028262G>A
CLNSRC
CLNACC RCV000481351.1, RCV000491172.1,