HMGB1, high mobility group box 1, 3146

N. diseases: 724; N. variants: 10
Disease: Mucocutaneous Lymph Node Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1412125
rs1412125
Entrez Id: 3146
Gene Symbol: HMGB1
HMGB1
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome 		0.010 GeneticVariation BEFREE The rs1412125 in HMGB1 might be a risk factor for the development of coronary artery lesions and IVIG resistance in KD patients. 30535242 2019