INSR, insulin receptor, 3643

N. diseases: 452; N. variants: 109
Disease: Severe 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: rs2229429
rs2229429 		1.000 0.040 19 7166377 missense variant G/A;C;T snv 0.20; 1.6E-05
CUI: C0271183
Disease: Severe myopia
Severe myopia 		Eye Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3745551
rs3745551 		1.000 0.040 19 7114277 3 prime UTR variant C/T snv 0.67
CUI: C0271183
Disease: Severe myopia
Severe myopia 		Eye Diseases 0.010 1.000 1 2015 2015