{{Rsnum
|rsid=255049
|Gene=DPEP3
|Chromosome=16
|position=67979568
|Orientation=plus
|GMAF=0.3127
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=DPEP3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 31.2 | 67.9
| HCB | 1.5 | 20.6 | 77.9
| JPT | 0.9 | 21.1 | 78.0
| YRI | 72.6 | 24.2 | 3.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 1.5 | 20.6 | 77.9
| CHD | 0.0 | 22.2 | 77.8
| GIH | 5.0 | 34.7 | 60.4
| LWK | 55.2 | 41.0 | 3.8
| MEX | 5.2 | 27.6 | 67.2
| MKK | 50.7 | 44.1 | 5.3
| TSI | 2.0 | 30.7 | 67.3
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19060910
|Trait=HDL cholesterol
|Title=Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
|RiskAllele=G
|Pval=3E-8
|OR=0.05
|ORtxt=[0.03-0.07] mmol/l increase
|OA=1
}}

{{PharmGKB
|RSID=rs255049
|Name_s=
|Gene_s=DPEP3
|Feature=
|Evidence=PubMed ID:19060910; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. (Initial Sample Size: 4,763 individuals; Replication Sample Size: NR); (Region: 16q22.1; Reported Gene(s): LCAT; Risk Allele: rs255049-G); (p-value= 0.00000003).This variant is associated with HDL cholesterol.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740272
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs255049
|overall_frequency_n=54
|overall_frequency_d=128
|overall_frequency=0.421875
|n_genomes=31
|n_genomes_annotated=0
|n_haplomes=45
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

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