{{Rsnum
|rsid=199476143
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=UGT1A12P
|position=1606
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=A
|CHROM=MT
|CLNACC=RCV000010156.1
|CLNALLE=1
|CLNDBN=Ataxia, progressive seizures, mental deterioration, and hearing loss
|CLNHGVS=NC_012920.1:m.1606G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=590105.0001
|Disease=Ataxia
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=1606
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476143
}}