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rs267607933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607933(A;C)
Make rs267607933(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414267
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607933
ebirs267607933
HLIrs267607933
Exacrs267607933
Varsomers267607933
Maprs267607933
PheGenIrs267607933
hapmaprs267607933
1000 genomesrs267607933
hgdprs267607933
ensemblrs267607933
gopubmedrs267607933
geneviewrs267607933
scholarrs267607933
googlers267607933
pharmgkbrs267607933
gwascentralrs267607933
openSNPrs267607933
23andMers267607933
23andMe allrs267607933
SNP Nexus

SNPshotrs267607933
SNPdbers267607933
MSV3drs267607933
GWAS Ctlgrs267607933
Max Magnitude0
ClinVar
Risk rs267607933(C;C)
Alt rs267607933(C;C)
Reference rs267607933(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641406A>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076714.2,