{{Rsnum
|rsid=121908579
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=BCS1L
|position=218661090
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=BCS1L,ZNF142
}}{{omim
|id=603647
|rsnum=121908579
|variant=0010
}}{{ClinVar
|rsid=121908579
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=219525813
|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.219525813G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000006548.1
|CLNDBN=BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603647.0010
|Disease=BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
}}