SF3B4, splicing factor 3b subunit 4, 10262

N. diseases: 110; N. variants: 22
Disease: hearing impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797045128
rs797045128
Entrez Id: 10262
Gene Symbol: SF3B4
SF3B4
CUI: C1384666
Disease:
hearing impairment 		T 0.700 CausalMutation CLINVAR