MLH1, mutL homolog 1, 4292

N. diseases: 526; N. variants: 757
Disease: Turcot syndrome (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751247
rs63751247
Entrez Id: 4292
Gene Symbol: MLH1
MLH1
CUI: C0265325
Disease:
Turcot syndrome (disorder) 		T 0.700 CausalMutation CLINVAR