rs869025222, RARB

N. diseases: 9
Disease: MICROPHTHALMIA, SYNDROMIC 12 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
MICROPHTHALMIA, SYNDROMIC 12
CUI: C3809803
Disease: MICROPHTHALMIA, SYNDROMIC 12
0.700 GeneticVariation CLINVAR Gain-of-Function Mutations in RARB Cause Intellectual Disability with Progressive Motor Impairment. 27120018 2016