Promoter region
SNP position
SNP ID
Gene
Disease
Type
P-value
Source
chr9:119449581-119463579
chr9:119462112
rs3019
TRIM32
Coronary heart disease
UTR-3
0.00039
GWASdb
chr9:119449581-119463579
chr9:119461680
rs17637172
LOC105376250
Cognitive decline rate in late mild cognitive impairment
intergenic_variant
2e-07
GWAS_Catalog