rs398124655, TAF2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40
CUI: C3810080
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40
0.700 GeneticVariation UNIPROT Microcephaly thin corpus callosum intellectual disability syndrome caused by mutated TAF2. 24084144 2013
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40
CUI: C3810080
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40
0.700 GeneticVariation UNIPROT Deep sequencing reveals 50 novel genes for recessive cognitive disorders. 21937992 2011