INSR, insulin receptor, 3643

N. diseases: 452; N. variants: 109
Disease: Compensatory Hyperinsulinemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2115386
rs2115386
Entrez Id: 3643
Gene Symbol: INSR
INSR
CUI: C1257965
Disease:
Compensatory Hyperinsulinemia 		0.010 GeneticVariation BEFREE The findings on INSR rs2115386 are supportive of the role of insulin resistance, or the compensatory hyperinsulinemia, in the pathogenesis of DR. 27768789 2016