rs634990, None

N. diseases: 6
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.
Abnormality of refraction
CUI: C4025843
Disease: Abnormality of refraction
31 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 0.700 1.000 1 2010 2010
Refractive Errors
CUI: C0034951
Disease: Refractive Errors
75 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 0.700 1.000 1 2010 2010
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 0.030 1.000 3 2011 2019
Myopia
CUI: C0027092
Disease: Myopia
167 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 0.020 1.000 2 2012 2018
Cataract
CUI: C0086543
Disease: Cataract
124 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 0.010 1.000 1 2011 2011
Hyperopia
CUI: C0020490
Disease: Hyperopia
29 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 0.010 1.000 1 2012 2012