{{Rsnum
|rsid=121908578
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=BCS1L
|position=218661848
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=BCS1L
}}{{omim
|id=603647
|rsnum=121908578
|variant=0009
}}{{ClinVar
|rsid=121908578
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=219526571
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=BCS1L:617
|GENE_NAME=BCS1L
|GENE_ID=617
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.219526571C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603647.0009
|CLNSIG=5
|CLNCUI=C1852372
|CLNDBN=BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY; Mitochondrial complex III deficiency
|Disease=BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY; Mitochondrial complex III deficiency
|CLNACC=RCV000006546.1; RCV000034811.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1852372:124000:254902
}}