INSR, insulin receptor, 3643

N. diseases: 452; N. variants: 109
Disease: Hyperinsulinemic Hypoglycemia, Familial, 5 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913156
rs121913156
Entrez Id: 3643
Gene Symbol: INSR
INSR
CUI: C1864952
Disease:
Hyperinsulinemic Hypoglycemia, Familial, 5 		T 0.700 CausalMutation CLINVAR
dbSNP: rs797045624
rs797045624
Entrez Id: 3643
Gene Symbol: INSR
INSR
CUI: C1864952
Disease:
Hyperinsulinemic Hypoglycemia, Familial, 5 		G 0.700 CausalMutation CLINVAR