CNTNAP2, contactin associated protein 2, 26047

N. diseases: 203; N. variants: 46
Disease: Specific language impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2710102
rs2710102
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
CUI: C0454651
Disease:
Specific language impairment 		0.010 GeneticVariation BEFREE Although association was found with rs2710102, the risk allele (a) for the traits studied here is the nonrisk allele for ASD and specific language impairment. 21193173 2011