rs751529077, MTUS1

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Blindness
CUI: C0456909
Disease: Blindness
0.010 GeneticVariation BEFREE The P28T carrier rate in this endogamous population is approximately 5%, suggesting that the mutation may be an important cause of early childhood blindness in countries with a sizeable Roma minority. 10521295 1999