Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064795591

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position47799916
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064795591
dbSNP (old)rs1064795591
ClinGenrs1064795591
ebirs1064795591
HLIrs1064795591
Exacrs1064795591
Gnomadrs1064795591
Varsomers1064795591
LitVarrs1064795591
Maprs1064795591
PheGenIrs1064795591
Biobankrs1064795591
1000 genomesrs1064795591
hgdprs1064795591
ensemblrs1064795591
gopubmedrs1064795591
geneviewrs1064795591
scholarrs1064795591
googlers1064795591
pharmgkbrs1064795591
gwascentralrs1064795591
openSNPrs1064795591
23andMers1064795591
23andMe allrs1064795591
SNPshotrs1064795591
SNPdbers1064795591
MSV3drs1064795591
GWAS Ctlgrs1064795591
Max Magnitude0
ClinVar
Risk rs1064795591(T;T)
Alt rs1064795591(T;T)
Reference Rs1064795591(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.48027055G>T
CLNSRC
CLNACC RCV000483556.1, RCV000490938.1,