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rs267607864

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607864(A;A)
Make rs267607864(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047610
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607864
ebirs267607864
HLIrs267607864
Exacrs267607864
Varsomers267607864
Maprs267607864
PheGenIrs267607864
hapmaprs267607864
1000 genomesrs267607864
hgdprs267607864
ensemblrs267607864
gopubmedrs267607864
geneviewrs267607864
scholarrs267607864
googlers267607864
pharmgkbrs267607864
gwascentralrs267607864
openSNPrs267607864
23andMers267607864
23andMe allrs267607864
SNP Nexus

SNPshotrs267607864
SNPdbers267607864
MSV3drs267607864
GWAS Ctlgrs267607864
Max Magnitude0
ClinVar
Risk rs267607864(A,T;A,T)
Alt rs267607864(A,T;A,T)
Reference rs267607864(C;C)
Significance Probable-Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37089101C>A; NC_000003.11:g.37089101C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075374.2, RCV000221100.1,