rs1538101, BNC2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Velopharyngeal dysfunction
CUI: C4280669
Disease: Velopharyngeal dysfunction
0.700 GeneticVariation GWASCAT GWAS reveals loci associated with velopharyngeal dysfunction. 29855589 2018