{{Rsnum
|rsid=212077
|Gene=ABCC6
|Chromosome=16
|position=16186919
|Orientation=plus
|GMAF=0.1171
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=ABCC6
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 61.1 | 36.3 | 2.7
| HCB | 91.0 | 9.0 | 0.0
| JPT | 82.3 | 17.7 | 0.0
| YRI | 90.3 | 9.0 | 0.7
| ASW | 84.2 | 15.8 | 0.0
| CHB | 91.0 | 9.0 | 0.0
| CHD | 93.5 | 6.5 | 0.0
| GIH | 68.4 | 29.6 | 2.0
| LWK | 85.3 | 14.7 | 0.0
| MEX | 75.4 | 24.6 | 0.0
| MKK | 71.5 | 27.8 | 0.7
| TSI | 59.8 | 33.3 | 6.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=20855565
|Title=Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease
|OA=1
}}
{{omim
|id=264800
|rsnum=212077
}}

{{ClinVar
|rsid=212077
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=16280776
|CHROM=16
|GMAF=0.1172
|dbSNPBuildID=79
|SSR=0
|SAO=0
|VP=0x05016808000115051f110100
|GENEINFO=ABCC6:368
|GENE_NAME=ABCC6
|GENE_ID=368
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.16280776G>C
|CLNORIGIN=0
|CLNSIG=1
|Tags=RV;PM;PMC;SLO;INT;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.8829; 0.1171
|COMMON=1
}}

{{PMID|19750004|OA=1
}} A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}