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rs267607691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607691(-;-)
Make rs267607691(-;CT)
Make rs267607691(CT;CT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475046
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607691
ebirs267607691
HLIrs267607691
Exacrs267607691
Varsomers267607691
Maprs267607691
PheGenIrs267607691
hapmaprs267607691
1000 genomesrs267607691
hgdprs267607691
ensemblrs267607691
gopubmedrs267607691
geneviewrs267607691
scholarrs267607691
googlers267607691
pharmgkbrs267607691
gwascentralrs267607691
openSNPrs267607691
23andMers267607691
23andMe allrs267607691
SNP Nexus

SNPshotrs267607691
SNPdbers267607691
MSV3drs267607691
GWAS Ctlgrs267607691
Max Magnitude0
ClinVar
Risk rs267607691(CT;CT)
Alt rs267607691(CT;CT)
Reference rs267607691(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702185_47702186insCT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076284.2,