{{Rsnum
|rsid=28934585
|Gene=ACADVL
|Chromosome=17
|position=7220519
|Orientation=plus
|GMAF=0.03076
|Gene_s=ACADVL,DLG4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{omim
|id=609575
|rsnum=28934585
|variant=0011
}}

{{ClinVar
|rsid=28934585
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=7123838
|CHROM=17
|GMAF=0.0307
|dbSNPBuildID=126
|SSR=0
|SAO=0
|VP=0x050160000000150516110100
|GENEINFO=DLG4:1742; ACADVL:37
|GENE_NAME=DLG4; ACADVL
|GENE_ID=1742; 37
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.7123838C>T
|CLNSRC=Emory University; GeneReviews; OMIM Allelic Variant
|CLNSRCID=1926; NBK6816; 609575.0011
|CLNSIG=5
|CLNCUI=C0342784
|CLNDBN=Very long chain acyl-CoA dehydrogenase deficiency; AllHighlyPenetrant
|Disease=Very long chain acyl-CoA dehydrogenase deficiency; AllHighlyPenetrant
|CLNACC=RCV000001698.1; RCV000020076.1; RCV000077913.1
|Tags=PM;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9692; 0.03076
|CLNDSDB=GeneReviews:MedGen:OMIM:OMIM:Orphanet:SNOMED_CT:SNOMED_CT; MedGen
|CLNDSDBID=NBK6816:C0342784:201460:201475:26793:237996001:237997005; CN169374
|COMMON=1
}}

{{GET Evidence
|gene=ACADVL
|aa_change=Pro65Leu
|aa_change_short=P65L
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs28934585
|overall_frequency_n=366
|overall_frequency_d=10758
|overall_frequency=0.0340212
|n_genomes=6
|n_genomes_annotated=0
|n_haplomes=6
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.025
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=7
|autoscore=3
|n_web_uneval=8
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}