CLDN14, claudin 14, 23562

N. diseases: 36; N. variants: 17
Disease: hearing impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204841
rs786204841
Entrez Id: 23562;105369301
Gene Symbol: CLDN14;LOC105369301
CLDN14;LOC105369301
CUI: C1384666
Disease:
hearing impairment 		T 0.700 GeneticVariation CLINVAR