Disease: Hypoglycemia, leucine-induced ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28936370
rs28936370
Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8
CUI: C0271714
Disease:
Hypoglycemia, leucine-induced 		0.800 GeneticVariation UNIPROT Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptor. 15356046 2004
dbSNP: rs28936370
rs28936370
Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8
CUI: C0271714
Disease:
Hypoglycemia, leucine-induced 		T 0.800 CausalMutation CLINVAR
dbSNP: rs1554948310
rs1554948310
Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8
CUI: C0271714
Disease:
Hypoglycemia, leucine-induced 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs193922402
rs193922402
Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8
CUI: C0271714
Disease:
Hypoglycemia, leucine-induced 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs72559715
rs72559715
Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8
CUI: C0271714
Disease:
Hypoglycemia, leucine-induced 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs72559722
rs72559722
Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8
CUI: C0271714
Disease:
Hypoglycemia, leucine-induced 		A 0.700 CausalMutation CLINVAR
dbSNP: rs72559734
rs72559734
Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8
CUI: C0271714
Disease:
Hypoglycemia, leucine-induced 		T 0.700 CausalMutation CLINVAR