{{Rsnum
|rsid=121908572
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=BCS1L
|position=218661283
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=BCS1L,ZNF142
}}{{omim
|id=603647
|rsnum=121908572
|variant=0002
}}{{ClinVar
|rsid=121908572
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=219526006
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ZNF142:7701; BCS1L:617
|GENE_NAME=ZNF142; BCS1L
|GENE_ID=7701; 617
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.219526006C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603647.0002
|CLNSIG=5
|CLNCUI=C1850598
|CLNDBN=Leigh syndrome due to mitochondrial complex III deficiency
|Disease=Leigh syndrome due to mitochondrial complex III deficiency
|CLNACC=RCV000006539.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1850598
}}