rs577948, MIR100HG

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, Degenerative
CUI: C0154778
Disease: Myopia, Degenerative
58 0.882 0.040 11 122159482 intron variant A/G snv 0.33 0.700 1.000 1 2009 2009
Myopia
CUI: C0027092
Disease: Myopia
167 0.882 0.040 11 122159482 intron variant A/G snv 0.33 0.020 2 2011 2014
Severe myopia
CUI: C0271183
Disease: Severe myopia
116 0.882 0.040 11 122159482 intron variant A/G snv 0.33 0.010 1.000 1 2010 2010