rs10824518, KCNMA1

N. diseases: 3
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 0.882 0.040 10 77303784 intron variant T/A;C snv 0.700 1.000 1 2016 2016
Myopic macular degeneration
CUI: C0730271
Disease: Myopic macular degeneration
4 0.882 0.040 10 77303784 intron variant T/A;C snv 0.010 1.000 1 2019 2019
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.882 0.040 10 77303784 intron variant T/A;C snv 0.010 1.000 1 2019 2019