rs77316810, RET

N. diseases: 10
Disease: Gastrointestinal symptom ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Gastrointestinal symptom
CUI: C0426576
Disease: Gastrointestinal symptom
0.010 GeneticVariation BEFREE We report an extensive molecular study of patients, two with HSCR and FMTC carrying a Cys620Arg or Ser mutation and two with MEN-2B and gastrointestinal symptoms carrying a Met918Thr mutation. 9681852 1998