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rs267607976

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607976(A;A)
Make rs267607976(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47471064
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607976
ebirs267607976
HLIrs267607976
Exacrs267607976
Varsomers267607976
Maprs267607976
PheGenIrs267607976
hapmaprs267607976
1000 genomesrs267607976
hgdprs267607976
ensemblrs267607976
gopubmedrs267607976
geneviewrs267607976
scholarrs267607976
googlers267607976
pharmgkbrs267607976
gwascentralrs267607976
openSNPrs267607976
23andMers267607976
23andMe allrs267607976
SNP Nexus

SNPshotrs267607976
SNPdbers267607976
MSV3drs267607976
GWAS Ctlgrs267607976
Max Magnitude0
ClinVar
Risk rs267607976(A,C;A,C)
Alt rs267607976(A,C;A,C)
Reference rs267607976(T;T)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47698203T>A; NC_000002.11:g.47698203T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076266.2, RCV000131428.2, RCV000076267.2,