Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs145606134
rs145606134
RAB40AL ; LINC00630
CUI: C0018775
Disease: Hearing Loss, Bilateral
Hearing Loss, Bilateral 		0.010 GeneticVariation BEFREE Our findings are inconsistent with a causative effect of RAB40AL p.D59G on cognitive impairment combined with severe to profound bilateral hearing loss but indicate that p.D59G is a common genetic variation. 25370018

2015