INS, insulin, 3630

N. diseases: 405; N. variants: 37
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: rs1057524907
rs1057524907
0.925 0.080 11 2159907 missense variant T/C snv
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
Nutritional and Metabolic Diseases 0.700 1.000 5 2007 2015
dbSNP: rs1564911425
rs1564911425
0.925 0.080 11 2159895 missense variant G/C snv
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
Nutritional and Metabolic Diseases 0.700 1.000 5 2007 2015