Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10487818
rs10487818
Entrez Id: 10135
Gene Symbol: NAMPT
NAMPT
CUI: C0028756
Disease:
Obesity, Morbid
0.010 GeneticVariation BEFREE One rare SNP, rs10487818, located in intron 4 of NAMPT was associated with severe obesity, with a minor allele frequency of 1.6% in controls, 0.4% in the class III obese adults and, remarkably, 0% in the severely obese children. 19300429 2009