rs28931594, GJB2

N. diseases: 9
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Keratitis
CUI: C0022568
Disease: Keratitis
0.010 GeneticVariation BEFREE Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome. 23924173 2013