rs765502229, IFI27

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Acromegaly
CUI: C0001206
Disease: Acromegaly
0.010 GeneticVariation BEFREE The I119T substitution occurred in a female patient with acromegaly. p27(I119T) shows an abnormal migration pattern by SDS-PAGE. 22291433 2012