ARHGAP32, Rho GTPase activating protein 32, 9743

N. diseases: 11; N. variants: 2
Disease: Alexithymia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002020
Disease: Alexithymia
Alexithymia 		0.010 Biomarker phenotype BEFREE From our analysis, variants in the genes ABCB4, TP53AIP1, ARHGAP32 and TMEM88B were identified linked to the alexithymia phenotype. 25882097 2015