rs8027411, ANKRD34C-AS1

N. diseases: 4
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.
Refractive Errors
CUI: C0034951
Disease: Refractive Errors
75 0.882 0.040 15 79168687 intron variant G/T snv 0.52 0.710 1.000 1 2010 2010
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.882 0.040 15 79168687 intron variant G/T snv 0.52 0.020 0.500 2 2011 2015
Cataract
CUI: C0086543
Disease: Cataract
124 0.882 0.040 15 79168687 intron variant G/T snv 0.52 0.010 1 2011 2011
Myopia
CUI: C0027092
Disease: Myopia
167 0.882 0.040 15 79168687 intron variant G/T snv 0.52 0.010 1.000 1 2018 2018