NTM, neurotrimin, 50863

N. diseases: 58; N. variants: 27
Disease: Myopia ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1793639
rs1793639 		1.000 0.040 11 132061637 intron variant G/A snv 0.39
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.700 1.000 1 2016 2016