GOLGA6A, golgin A6 family member A, 342096

N. diseases: 90; N. variants: 1
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: rs747797174
rs747797174 		0.925 0.040 15 74070978 missense variant C/A;G;T snv 1.2E-05
CUI: C0271183
Disease: Severe myopia
Severe myopia 		Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs747797174
rs747797174 		0.925 0.040 15 74070978 missense variant C/A;G;T snv 1.2E-05
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.010 1.000 1 2019 2019