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rs267607869

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607869(C;C)
Make rs267607869(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047685
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607869
ebirs267607869
HLIrs267607869
Exacrs267607869
Varsomers267607869
Maprs267607869
PheGenIrs267607869
hapmaprs267607869
1000 genomesrs267607869
hgdprs267607869
ensemblrs267607869
gopubmedrs267607869
geneviewrs267607869
scholarrs267607869
googlers267607869
pharmgkbrs267607869
gwascentralrs267607869
openSNPrs267607869
23andMers267607869
23andMe allrs267607869
SNP Nexus

SNPshotrs267607869
SNPdbers267607869
MSV3drs267607869
GWAS Ctlgrs267607869
Max Magnitude0
ClinVar
Risk rs267607869(C;C)
Alt rs267607869(C;C)
Reference rs267607869(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089176T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075407.2,