{{Rsnum
|rsid=6083
|Gene=LIPC
|Chromosome=15
|position=58545811
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.4118
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=LIPC
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 44.2 | 40.7 | 15.0
| HCB | 3.7 | 33.8 | 62.5
| JPT | 0.0 | 10.6 | 89.4
| YRI | 7.5 | 46.3 | 46.3
| ASW | 7.0 | 42.1 | 50.9
| CHB | 3.7 | 33.8 | 62.5
| CHD | 2.8 | 33.3 | 63.9
| GIH | 24.8 | 45.5 | 29.7
| LWK | 7.3 | 49.1 | 43.6
| MEX | 19.0 | 53.4 | 27.6
| MKK | 9.7 | 45.2 | 45.2
| TSI | 47.5 | 47.5 | 5.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=6083
|allele=G
|frequency=0.417
|uid=1103645624024
|type=homozygous_SNP
|hugo=LIPC
|ensembl gene=ENSG00000166035
|ensembl transcript=ENST00000299022
|sift=AFFECT FUNCTION
|disease=Defects in LIPC are the cause of hepatic lipase deficiency (HL deficiency) (MIM:151670).
}}

{{PMID Auto
|PMID=16700901
|Title=Physiogenomic analysis of weight loss induced by dietary carbohydrate restriction.
|OA=1
}}

{{PMID Auto
|PMID=18076107
|Title=Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis.
|OA=1
}}

{{GET Evidence
|gene=LIPC
|aa_change=Asn215Ser
|aa_change_short=N215S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6083
|overall_frequency_n=5029
|overall_frequency_d=10758
|overall_frequency=0.467466
|n_genomes=50
|n_genomes_annotated=0
|n_haplomes=73
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.002
|nblosum100=0
|autoscore=0
|webscore=N
}}

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