{{Rsnum
|rsid=3829462
|Gene=LIPC
|Chromosome=15
|position=58560880
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=A
|GMAF=0.06979
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=LIPC
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.0 | 2.7 | 97.3
| HCB | 0.0 | 14.7 | 85.3
| JPT | 0.9 | 24.1 | 75.0
| YRI | 0.7 | 26.7 | 72.6
| ASW | 1.8 | 31.6 | 66.7
| CHB | 0.0 | 14.7 | 85.3
| CHD | 0.0 | 8.3 | 91.7
| GIH | 0.0 | 3.0 | 97.0
| LWK | 7.3 | 30.0 | 62.7
| MEX | 0.0 | 0.0 | 0.0
| MKK | 1.3 | 17.3 | 81.4
| TSI | 0.0 | 2.0 | 98.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=3829462
|allele=A
|frequency=0.025
|uid=1103645624063
|type=heterozygous_SNP
|hugo=LIPC
|ensembl gene=ENSG00000166035
|ensembl transcript=ENST00000299022
|sift=
|disease=Defects in LIPC are the cause of hepatic lipase deficiency (HL deficiency) (MIM:151670).
}}

{{PMID|17903301|OA=1
}} Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.

{{PMID|19041386|OA=1
}} Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.

{{GET Evidence
|gene=LIPC
|aa_change=Phe356Leu
|aa_change_short=F356L
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3829462
|overall_frequency_n=10182
|overall_frequency_d=10758
|overall_frequency=0.946458
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=105
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}