rs1355262412, USH1C

N. diseases: 3
Disease: Deafness, Autosomal Recessive 18 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Deafness, Autosomal Recessive 18
CUI: C1865870
Disease: Deafness, Autosomal Recessive 18
0.700 GeneticVariation CLINVAR Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease. 28041643 2017