{{Rsnum
|rsid=6979
|Gene=ACD
|Chromosome=16
|position=67657765
|Orientation=plus
|GMAF=0.4812
|Gene_s=ACD,RLTPR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 26.5 | 55.8 | 17.7
| HCB | 73.0 | 24.8 | 2.2
| JPT | 74.3 | 22.1 | 3.5
| YRI | 0.0 | 0.7 | 99.3
| ASW | 1.8 | 19.3 | 78.9
| CHB | 73.0 | 24.8 | 2.2
| CHD | 64.8 | 28.7 | 6.5
| GIH | 19.8 | 50.5 | 29.7
| LWK | 0.0 | 2.7 | 97.3
| MEX | 40.4 | 42.1 | 17.5
| MKK | 0.0 | 12.8 | 87.2
| TSI | 18.6 | 47.1 | 34.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=19854717
|Title=The chromosome 16q region associated with ankylosing spondylitis includes the candidate gene tumour necrosis factor receptor type 1-associated death domain (TRADD)
|OA=1
}}

{{GET Evidence
|gene=ACD
|aa_change=Val518Ala
|aa_change_short=V518A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6979
|overall_frequency_n=6728
|overall_frequency_d=10758
|overall_frequency=0.625395
|n_genomes=44
|n_genomes_annotated=0
|n_haplomes=69
|n_articles=0
|n_articles_annotated=0
|nblosum100=2
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}