{{Rsnum
|rsid=121908571
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=BCS1L
|position=218662620
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=BCS1L
}}{{omim
|id=603647
|rsnum=121908571
|variant=0001
}}{{ClinVar
|rsid=121908571
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=219527343
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=BCS1L:617
|GENE_NAME=BCS1L
|GENE_ID=617
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.219527343G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603647.0001
|CLNSIG=5
|CLNCUI=C1852372
|CLNDBN=Mitochondrial complex III deficiency
|Disease=Mitochondrial complex III deficiency
|CLNACC=RCV000006538.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1852372:124000:254902
}}