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rs267607806

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607806(C;C)
Make rs267607806(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37017601
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607806
ebirs267607806
HLIrs267607806
Exacrs267607806
Varsomers267607806
Maprs267607806
PheGenIrs267607806
hapmaprs267607806
1000 genomesrs267607806
hgdprs267607806
ensemblrs267607806
gopubmedrs267607806
geneviewrs267607806
scholarrs267607806
googlers267607806
pharmgkbrs267607806
gwascentralrs267607806
openSNPrs267607806
23andMers267607806
23andMe allrs267607806
SNP Nexus

SNPshotrs267607806
SNPdbers267607806
MSV3drs267607806
GWAS Ctlgrs267607806
Max Magnitude0
ClinVar
Risk rs267607806(C;C)
Alt rs267607806(C;C)
Reference rs267607806(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059092T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075904.2,