{{Rsnum
|rsid=387906217
|Chromosome=20
|Orientation=minus
|geno1=(GA;GA)
|geno2=(GA;TTT)
|geno3=(TTT;TTT)
|Gene=ABHD12
|position=25323409
|Gene_s=ABHD12
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=AAAA
|CHROM=20
|CLNACC=RCV000000041.1
|CLNALLE=1
|CLNDBN=Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2675204:612674:171848
|CLNHGVS=NC_000020.10:g.25304045_25304046delTCinsAAA
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613599.0001
|Disease=Polyneuropathy
|FwdALT=TTT
|FwdREF=GA
|REF=ATC
|RSPOS=25304044
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906217
|GENEINFO=ABHD12:26090
|GENE_ID=26090
|GENE_NAME=ABHD12
}}