{{Rsnum
|rsid=137853192
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SDHAF1
|position=35995443
|Gene_s=SDHAF1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=612848
|variant=0001
|rsnum=137853192
}}{{ClinVar
|rsid=137853192
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=36486345
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SDHAF1:644096
|GENE_NAME=SDHAF1
|GENE_ID=644096
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.36486345G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612848.0001
|CLNSIG=5
|CLNCUI=C1855008
|CLNDBN=Mitochondrial complex II deficiency
|Disease=Mitochondrial complex II deficiency
|CLNACC=RCV000000457.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1855008:252011
}}