Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs748718975
rs748718975
Entrez Id: 1805
Gene Symbol: DPT
DPT
CUI: C1843156
Disease:
Progressive sensorineural hearing impairment
A 0.700 CausalMutation CLINVAR Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease. 27876815 2017