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

rs1064794809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position47414347
GeneMSH2
is asnp
is mentioned by
dbSNPrs1064794809
dbSNP (old)rs1064794809
ClinGenrs1064794809
ebirs1064794809
HLIrs1064794809
Exacrs1064794809
Gnomadrs1064794809
Varsomers1064794809
Maprs1064794809
PheGenIrs1064794809
Biobankrs1064794809
1000 genomesrs1064794809
hgdprs1064794809
ensemblrs1064794809
gopubmedrs1064794809
geneviewrs1064794809
scholarrs1064794809
googlers1064794809
pharmgkbrs1064794809
gwascentralrs1064794809
openSNPrs1064794809
23andMers1064794809
23andMe allrs1064794809
SNPshotrs1064794809
SNPdbers1064794809
MSV3drs1064794809
GWAS Ctlgrs1064794809
Max Magnitude0
ClinVar
Risk rs1064794809(-;-)
Alt rs1064794809(-;-)
Reference Rs1064794809(C;C)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47641486delC
CLNSRC
CLNACC RCV000484912.1, RCV000491867.1,