{{Rsnum
|rsid=3812153
|Gene=ELOVL4
|Chromosome=6
|position=79916658
|Orientation=minus
|GMAF=0.1864
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ELOVL4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 75.2 | 22.1 | 2.7
| HCB | 65.2 | 30.4 | 4.4
| JPT | 64.3 | 32.1 | 3.6
| YRI | 53.1 | 37.2 | 9.7
| ASW | 59.6 | 35.1 | 5.3
| CHB | 65.2 | 30.4 | 4.4
| CHD | 67.9 | 29.4 | 2.8
| GIH | 39.4 | 43.4 | 17.2
| LWK | 50.9 | 43.6 | 5.5
| MEX | 65.5 | 32.8 | 1.7
| MKK | 68.4 | 25.2 | 6.5
| TSI | 82.4 | 15.7 | 2.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=3812153
|allele=C
|frequency=0.167
|uid=1103652914136
|type=heterozygous_SNP
|hugo=ELOVL4
|ensembl gene=ENSG00000118402
|ensembl transcript=ENST00000369816
|sift=TOLERATED
|disease=Defects in ELOVL4 are a cause of autosomal dominant Stargardt-like macular dystrophy (ADMD) (MIM:600110).
}}

{{PMID Auto
|PMID=20388345
|Title=[Association of M299V variant in ELOVL4 gene with exudative age-related macular degeneration in a Chinese population].
}}

{{GET Evidence
|gene=ELOVL4
|aa_change=Met299Val
|aa_change_short=M299V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3812153
|overall_frequency_n=1611
|overall_frequency_d=10758
|overall_frequency=0.149749
|n_genomes=17
|n_genomes_annotated=0
|n_haplomes=19
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=0
|autoscore=2
|n_web_uneval=10
}}

{{PMID Auto
|PMID=22948568
|Title=Evaluation of the ELOVL4, PRPH2 and ABCA4 genes in patients with Stargardt             macular degeneration
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}