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rs267607987

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607987(C;C)
Make rs267607987(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475272
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607987
ebirs267607987
HLIrs267607987
Exacrs267607987
Varsomers267607987
Maprs267607987
PheGenIrs267607987
hapmaprs267607987
1000 genomesrs267607987
hgdprs267607987
ensemblrs267607987
gopubmedrs267607987
geneviewrs267607987
scholarrs267607987
googlers267607987
pharmgkbrs267607987
gwascentralrs267607987
openSNPrs267607987
23andMers267607987
23andMe allrs267607987
SNP Nexus

SNPshotrs267607987
SNPdbers267607987
MSV3drs267607987
GWAS Ctlgrs267607987
Max Magnitude0
ClinVar
Risk rs267607987(C;C)
Alt rs267607987(C;C)
Reference rs267607987(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702411T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076341.2,