{{Rsnum
|rsid=12093699
|Chromosome=1
|position=159678198
|Orientation=plus
|GMAF=0.2553
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 8.8 | 44.2 | 46.9
| HCB | 0.0 | 13.9 | 86.1
| JPT | 0.9 | 9.7 | 89.4
| YRI | 14.5 | 37.9 | 47.6
| ASW | 14.0 | 26.3 | 59.6
| CHB | 0.0 | 13.9 | 86.1
| CHD | 0.9 | 13.0 | 86.1
| GIH | 5.0 | 29.7 | 65.3
| LWK | 18.3 | 35.8 | 45.9
| MEX | 8.6 | 46.6 | 44.8
| MKK | 14.1 | 50.6 | 35.3
| TSI | 13.7 | 34.3 | 52.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18464913
|Trait=Protein quantitative trait loci
|Title=A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
|RiskAllele=
|Pval=0.0000060000000000000002
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID|18464913|OA=1
}} C-reactive protein ([[CRP]]) levels

{{PharmGKB
|RSID=rs12093699
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:18439552
|Annotation=In a GWAS of subjects from the PARC study (Pharmacogenomics and Risk of Cardiovascular Disease), this was one of the ten SNPs most strongly associated with plasma C-reactive protein levels.
|Drugs=
|Drug Classes=
|Diseases=Cardiovascular Diseases
|Curation Level=Curated
|PharmGKB Accession ID=PA162399733
}}

{{PMID Auto
|PMID=18216863
|Title=Genetic determinants of basal C-reactive protein expression in Filipino systemic lupus erythematosus families.
|OA=1
}}

{{PMID Auto
|PMID=18439548
|Title=Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=18500540
|Title=Fine-mapping the genetic basis of CRP regulation in African Americans: a Bayesian approach.
|OA=1
}}

{{PMID Auto
|PMID=18853133
|Title=Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12093699
|overall_frequency_n=32
|overall_frequency_d=128
|overall_frequency=0.25
|n_genomes=20
|n_genomes_annotated=0
|n_haplomes=23
|n_articles=1
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}