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rs267607831

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607831(G;G)
Make rs267607831(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028934
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607831
ebirs267607831
HLIrs267607831
Exacrs267607831
Varsomers267607831
Maprs267607831
PheGenIrs267607831
hapmaprs267607831
1000 genomesrs267607831
hgdprs267607831
ensemblrs267607831
gopubmedrs267607831
geneviewrs267607831
scholarrs267607831
googlers267607831
pharmgkbrs267607831
gwascentralrs267607831
openSNPrs267607831
23andMers267607831
23andMe allrs267607831
SNP Nexus

SNPshotrs267607831
SNPdbers267607831
MSV3drs267607831
GWAS Ctlgrs267607831
Max Magnitude0
ClinVar
Risk rs267607831(G;G)
Alt rs267607831(G;G)
Reference rs267607831(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070425T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075248.2,