Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs144169475
rs144169475
Entrez Id: 152518
Gene Symbol: NFXL1
NFXL1
CUI: C0023015
Disease:
Language Disorders 		0.010 GeneticVariation BEFREE We then apply association analyses across the wider population to highlight a single rare coding variant (rs144169475, Minor Allele Frequency of 4.1% in admixed South American populations) in the NFXL1 gene that confers a nonsynonymous change (N150K) and is significantly associated with language impairment in the Robinson Crusoe population (p = 2.04 × 10-4, 8 variants tested). 25781923 2015