Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398124655
rs398124655
Entrez Id: 6873
Gene Symbol: TAF2
TAF2
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
dbSNP: rs398124655
rs398124655
Entrez Id: 6873
Gene Symbol: TAF2
TAF2
CUI: C3810080
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40
0.700 GeneticVariation UNIPROT Deep sequencing reveals 50 novel genes for recessive cognitive disorders. 21937992 2011