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rs267608011

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267608011(A;C)
Make rs267608011(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47480694
GeneMSH2
is asnp
is mentioned by
dbSNPrs267608011
dbSNP (old)rs267608011
ClinGenrs267608011
ebirs267608011
HLIrs267608011
Exacrs267608011
Gnomadrs267608011
Varsomers267608011
Maprs267608011
PheGenIrs267608011
Biobankrs267608011
1000 genomesrs267608011
hgdprs267608011
ensemblrs267608011
gopubmedrs267608011
geneviewrs267608011
scholarrs267608011
googlers267608011
pharmgkbrs267608011
gwascentralrs267608011
openSNPrs267608011
23andMers267608011
23andMe allrs267608011
SNPshotrs267608011
SNPdbers267608011
MSV3drs267608011
GWAS Ctlgrs267608011
Max Magnitude0
ClinVar
Risk rs267608011(C;C) rs267608011(G;G)
Alt rs267608011(C;C) rs267608011(G;G)
Reference Rs267608011(A;A)
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.47707833A>G
CLNSRC
CLNACC RCV000478491.1, RCV000491654.1,