Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555611722
rs1555611722
0.800 GeneticVariation UNIPROT A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development. 29463886

2019

dbSNP: rs1555611722
rs1555611722
0.800 GeneticVariation UNIPROT CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. 30397230

2018