rs28935498, FGD1

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
MENTAL RETARDATION, X-LINKED, SYNDROMIC 16
CUI: C3275558
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC 16
0.700 CausalMutation CLINVAR
Mental Retardation, X-Linked
CUI: C1136249
Disease: Mental Retardation, X-Linked
0.010 GeneticVariation BEFREE Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene. 11940089 2002