rs121917843, PROP1

N. diseases: 3
Disease: Panhypopituitarism ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Panhypopituitarism
CUI: C0242343
Disease: Panhypopituitarism
0.010 GeneticVariation BEFREE The p.R73C PROP1 mutation was the most frequent mutation in CPHD; this should be the first one to screen in this population. 25557026 2015