rs747797174, GOLGA6A

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Myopia
CUI: C0027092
Disease: Myopia
167 0.925 0.040 15 74070978 missense variant C/A;G;T snv 1.2E-05 0.010 1.000 1 2019 2019
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.925 0.040 15 74070978 missense variant C/A;G;T snv 1.2E-05 0.010 1.000 1 2019 2019