S100A9, S100 calcium binding protein A9, 6280

N. diseases: 363; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2916193
rs2916193
Entrez Id: 6280
Gene Symbol: S100A9
S100A9
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs3014866
rs3014866
Entrez Id: 6280
Gene Symbol: S100A9
S100A9
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 GeneticVariation BEFREE The minor allele (T) of the S100A9 variant rs3014866 is associated with lower T2D risk in 3 populations of different ancestries. 27440084 2016
dbSNP: rs3014866
rs3014866
Entrez Id: 6280
Gene Symbol: S100A9
S100A9
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 GeneticVariation BEFREE The rs3014866 SNP was associated with circulating S100A9 and the risk of T2D, having TT carriers at 28 % (p = 0.03) lower risk (n = 1,450). 23207880 2013