{{Rsnum
|rsid=12713559
|Gene=APOB
|Chromosome=2
|position=21006196
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=APOB
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 97.3 | 2.7 | 0.0
| MEX | 96.5 | 3.5 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{ population diversity
| geno1 = (C;C)
| geno2 = 
| geno3 = 
| CEU | 100.0 | 0 | 0
| CHB | 100.0 | 0 | 0
| JPT | 100.0 | 0 | 0
| YRI | 100.0 | 0 | 0
}}

{{omim
|id=107730
|rsnum=12713559
|variant=0017
}}

{{ClinVar
|rsid=12713559
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=21229068
|CHROM=2
|GMAF=0.0005
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050170000000040517110100
|GENEINFO=APOB:338
|GENE_NAME=APOB
|GENE_ID=338
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.21229068G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;TPA;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9995; 0.0004591
|CLNACC=RCV000019486.26
|CLNDBN=Familial hypercholesterolemia
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=107730.0017
|COMMON=0
|Disease=Familial hypercholesterolemia
|CLNDSDB=MedGen:OMIM:OMIM:SNOMED_CT:SNOMED_CT
|CLNDSDBID=C0020445:143890:144400:397915002:398036000
}}

[[Familial Hypercholesterolemia Type B]]

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