SPATA5, spermatogenesis associated 5, 166378

N. diseases: 75; N. variants: 26
Disease: Cortical visual impairment ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs796052243
rs796052243
Entrez Id: 166378
Gene Symbol: SPATA5
SPATA5
CUI: C4048268
Disease:
Cortical visual impairment 		T 0.700 GeneticVariation CLINVAR