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rs267607934

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607934(A;A)
Make rs267607934(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412561
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607934
ebirs267607934
HLIrs267607934
Exacrs267607934
Varsomers267607934
Maprs267607934
PheGenIrs267607934
hapmaprs267607934
1000 genomesrs267607934
hgdprs267607934
ensemblrs267607934
gopubmedrs267607934
geneviewrs267607934
scholarrs267607934
googlers267607934
pharmgkbrs267607934
gwascentralrs267607934
openSNPrs267607934
23andMers267607934
23andMe allrs267607934
SNP Nexus

SNPshotrs267607934
SNPdbers267607934
MSV3drs267607934
GWAS Ctlgrs267607934
Max Magnitude0
ClinVar
Risk rs267607934(A;A)
Alt rs267607934(A;A)
Reference rs267607934(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639700G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076709.2,