Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs483352866
rs483352866
TBC1D24
0.800 GeneticVariation UNIPROT TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss. 24729539

2014
dbSNP: rs483352866
rs483352866
TBC1D24
0.800 GeneticVariation UNIPROT A dominant mutation in the stereocilia-expressing gene TBC1D24 is a probable cause for nonsyndromic hearing impairment. 24729547

2014
dbSNP: rs483352866
rs483352866
TBC1D24
T 0.800 CausalMutation CLINVAR