CLDN14, claudin 14, 23562

N. diseases: 36; N. variants: 17
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 29 ×
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: C3279660
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 29 		T 0.800 GeneticVariation CLINVAR
dbSNP: rs786204841
rs786204841
Entrez Id: 23562;105369301
Gene Symbol: CLDN14;LOC105369301
CLDN14;LOC105369301
CUI: C3279660
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 29 		0.800 GeneticVariation UNIPROT
dbSNP: rs786204841
rs786204841
Entrez Id: 23562;105369301
Gene Symbol: CLDN14;LOC105369301
CLDN14;LOC105369301
CUI: C3279660
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 29 		T 0.800 CausalMutation CLINVAR