{{Rsnum
|rsid=679899
|Gene=APOB
|Chromosome=2
|position=21028042
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.4917
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=APOB
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 20.9 | 48.2 | 30.9
| HCB | 76.5 | 21.2 | 2.3
| JPT | 78.8 | 19.5 | 1.8
| YRI | 1.4 | 20.0 | 78.6
| ASW | 1.8 | 28.6 | 69.6
| CHB | 76.5 | 21.2 | 2.3
| CHD | 75.5 | 17.9 | 6.6
| GIH | 42.7 | 44.8 | 12.5
| LWK | 1.9 | 20.8 | 77.4
| MEX | 22.2 | 40.7 | 37.0
| MKK | 5.3 | 34.2 | 60.5
| TSI | 20.4 | 51.0 | 28.6
| HapMapRevision=28
}}

{{Venter SNP
|rsid=679899
|allele=A
|frequency=
|uid=1103658040725
|type=heterozygous_SNP
|hugo=APOB
|ensembl gene=ENSG00000084674
|ensembl transcript=ENST00000381043
|sift=TOLERATED
|disease=Defects in APOB associated with defects in other genes (polygenic) can contribute to hypocholesterolemia.
}}

{{PMID Auto
|PMID=19282863
|Title=Association of candidate gene polymorphisms with chronic kidney disease in Japanese individuals with hypertension
}}

{{PMID Auto
|PMID=20018037
|Title=Mendelian randomization in family data.
|OA=1
}}

{{GET Evidence
|gene=APOB
|aa_change=Ala618Val
|aa_change_short=A618V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs679899
|overall_frequency_n=3942
|overall_frequency_d=10758
|overall_frequency=0.366425
|n_genomes=26
|n_genomes_annotated=0
|n_haplomes=43
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=2
|autoscore=2
|n_web_uneval=3
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}