rs11567847, TEAD1

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Disorder of eye
CUI: C0015397
Disease: Disorder of eye
0.010 GeneticVariation BEFREE A mutation in the TEAD1 gene, Tyr421His, has been identified in patients suffering from Sveinsson's chorioretinal atrophy (SCA), an autosomal dominant eye disease. 30903741 2019