SPATA22, spermatogenesis associated 22, 84690

N. diseases: 6; N. variants: 65
Disease: Myopia, Degenerative ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs923375
rs923375 		1.000 0.040 17 3489774 intron variant T/C;G snv
CUI: C0154778
Disease: Myopia, Degenerative
Myopia, Degenerative 		Eye Diseases 0.700 1.000 1 2012 2012