Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1568839335
rs1568839335
Entrez Id: 23562;105369301
Gene Symbol: CLDN14;LOC105369301
CLDN14;LOC105369301
CUI: C3279660
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 29
T 0.700 GeneticVariation CLINVAR