{{Rsnum
|rsid=199476144
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=UGT1A12P
|position=1624
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=T
|CHROM=MT
|CLNACC=RCV000010157.3; RCV000010158.1
|CLNALLE=1
|CLNDBN=Neonatal death; Leigh's disease
|CLNDSDB=MedGen; GeneReviews:GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0410916; NBK1173:NBK1203:NBK1224:C0023264:256000:ORPHA506:29570005
|CLNHGVS=NC_012920.1:m.1624C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=590105.0002
|Disease=Neonatal death; Leigh's disease
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=1624
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476144
}}