Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1130864
rs1130864
CRP
0.020 GeneticVariation BEFREE The present case control study investigated the contribution of three relevant CRP single nucleotide polymorphisms: -717A>G located in the promoter region (rs2794521), +1059G>C on exon2 (rs1800947) and +1444C>T in the 3' UTR (rs1130864) in 180 angiographically verified CHD cases and 175 control subjects. 24965144

2014
dbSNP: rs1130864
rs1130864
CRP
0.020 GeneticVariation BEFREE We found no association of a genetic variant, which is known to be related to CRP levels, (rs1130864) and having CHD. 18714384

2008