RAD51B, RAD51 paralog B, 5890

N. diseases: 126; N. variants: 108
Disease: Meigs Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025184
Disease: Meigs Syndrome
Meigs Syndrome 		0.010 GeneticVariation disease BEFREE This observation supports a model in which accumulation of two independent mutations-a classical structural rearrangement involving HMGA2 and RAD51L1, in combination with a loss of the second RAD51L1 allele-might play a major role in the development of pseudo-Meigs' syndrome. 11746973 2001