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rs1064795256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position47799697
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064795256
dbSNP (old)rs1064795256
ClinGenrs1064795256
ebirs1064795256
HLIrs1064795256
Exacrs1064795256
Gnomadrs1064795256
Varsomers1064795256
Maprs1064795256
PheGenIrs1064795256
Biobankrs1064795256
1000 genomesrs1064795256
hgdprs1064795256
ensemblrs1064795256
gopubmedrs1064795256
geneviewrs1064795256
scholarrs1064795256
googlers1064795256
pharmgkbrs1064795256
gwascentralrs1064795256
openSNPrs1064795256
23andMers1064795256
23andMe allrs1064795256
SNPshotrs1064795256
SNPdbers1064795256
MSV3drs1064795256
GWAS Ctlgrs1064795256
Max Magnitude0
ClinVar
Risk rs1064795256(G;G) rs1064795256(T;T)
Alt rs1064795256(G;G) rs1064795256(T;T)
Reference Rs1064795256(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48026836C>G; NC_000002.11:g.48026836C>T
CLNSRC
CLNACC RCV000491403.1, RCV000487144.1,