rs121909049, HSF4

N. diseases: 1
Disease: CATARACT 5, MULTIPLE TYPES ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
CATARACT 5, MULTIPLE TYPES
CUI: C3888417
Disease: CATARACT 5, MULTIPLE TYPES
0.800 GeneticVariation UNIPROT Novel HSF4 mutation causes congenital total white cataract in a Chinese family. 16876512 2006
CATARACT 5, MULTIPLE TYPES
CUI: C3888417
Disease: CATARACT 5, MULTIPLE TYPES
0.800 GeneticVariation UNIPROT Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract. 12089525 2002
CATARACT 5, MULTIPLE TYPES
CUI: C3888417
Disease: CATARACT 5, MULTIPLE TYPES
0.800 CausalMutation CLINVAR