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rs267607822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267607822(-;-)
Make rs267607822(-;T)
Make rs267607822(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position37025644
GeneMLH1
is asnp
is mentioned by
dbSNPrs267607822
ebirs267607822
HLIrs267607822
Exacrs267607822
Varsomers267607822
Maprs267607822
PheGenIrs267607822
hapmaprs267607822
1000 genomesrs267607822
hgdprs267607822
ensemblrs267607822
gopubmedrs267607822
geneviewrs267607822
scholarrs267607822
googlers267607822
pharmgkbrs267607822
gwascentralrs267607822
openSNPrs267607822
23andMers267607822
23andMe allrs267607822
SNP Nexus

SNPshotrs267607822
SNPdbers267607822
MSV3drs267607822
GWAS Ctlgrs267607822
Max Magnitude0
ClinVar
Risk rs267607822(T;T)
Alt rs267607822(T;T)
Reference rs267607822(;)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.37067135dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075099.2, RCV000166148.1,