{{Rsnum
|rsid=2277862
|Gene=FER1L4
|Chromosome=20
|position=35564866
|Orientation=minus
|GMAF=0.1474
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=FER1L4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 22.3 | 76.8
| HCB | 3.0 | 21.5 | 75.6
| JPT | 0.9 | 15.0 | 84.1
| YRI | 5.4 | 33.3 | 61.2
| ASW | 5.3 | 24.6 | 70.2
| CHB | 3.0 | 21.5 | 75.6
| CHD | 2.8 | 29.4 | 67.9
| GIH | 10.0 | 45.0 | 45.0
| LWK | 1.8 | 24.5 | 73.6
| MEX | 1.7 | 19.0 | 79.3
| MKK | 5.8 | 35.3 | 59.0
| TSI | 4.9 | 34.3 | 60.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20686565
|Trait=None
|Title=Biological, clinical and population relevance of 95 loci for blood lipids.
|RiskAllele=T
|Pval=4E-10
|OR=1.1900
|ORtxt=None
|OA=1
}}

{{GET Evidence
|gene=FER1L4
|aa_change=Val665Ile
|aa_change_short=V665I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2277862
|overall_frequency_n=18
|overall_frequency_d=128
|overall_frequency=0.140625
|n_genomes=13
|n_genomes_annotated=0
|n_haplomes=16
|n_articles=0
|n_articles_annotated=0
|nblosum100=-4
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}