rs587779139, MSH2

N. diseases: 4
Disease: Lynch Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
0.010 GeneticVariation BEFREE The nonsense mutation MSH2 c.2152C>T shows a founder effect in Portuguese Lynch syndrome families. 30968502 2019