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rs267607842

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607842(A;A)
Make rs267607842(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37040241
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607842
ebirs267607842
HLIrs267607842
Exacrs267607842
Varsomers267607842
Maprs267607842
PheGenIrs267607842
hapmaprs267607842
1000 genomesrs267607842
hgdprs267607842
ensemblrs267607842
gopubmedrs267607842
geneviewrs267607842
scholarrs267607842
googlers267607842
pharmgkbrs267607842
gwascentralrs267607842
openSNPrs267607842
23andMers267607842
23andMe allrs267607842
SNP Nexus

SNPshotrs267607842
SNPdbers267607842
MSV3drs267607842
GWAS Ctlgrs267607842
Max Magnitude0
ClinVar
Risk rs267607842(A;A)
Alt rs267607842(A;A)
Reference rs267607842(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081732G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075277.2,