HMGA1, high mobility group AT-hook 1, 3159

N. diseases: 206; N. variants: 5
Disease: Metabolic Syndrome X ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs146052672
rs146052672
Entrez Id: 3159
Gene Symbol: HMGA1
HMGA1
CUI: C0524620
Disease:
Metabolic Syndrome X 		0.010 GeneticVariation BEFREE Overall, our results indicate that the rs146052672</span> variant represents an early predictive marker of MetS, as well as a predictive tool for therapy. 23512162 2013