{{Rsnum
|rsid=568413
|Gene=APOB
|Chromosome=2
|position=21012603
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 97.8 | 2.2 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 99.3 | 0.7 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 97.8 | 2.2 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 96.6 | 3.4 | 0.0
| MKK | 99.4 | 0.6 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=568413
|allele=C
|frequency=1
|uid=1103658040696
|type=homozygous_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.
}}

{{GET Evidence
|gene=APOB
|aa_change=Tyr1422Cys
|aa_change_short=Y1422C
|impact=benign
|qualified_impact=Low clinical importance, Uncertain benign
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs568413
|overall_frequency_n=10744
|overall_frequency_d=10748
|overall_frequency=0.999628
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=112
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=5
|qualitycomment_in_silico=Y
|qualityscore_in_vitro=0
|qualityscore_case_control=5
|qualitycomment_case_control=Y
|qualityscore_familial=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=6
|autoscore=2
|n_web_uneval=1
|variant_evidence=0
|clinical_importance=0
|summary_short=This position is almost certainly an error in the HG18 reference sequence. 
}}

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