{{Rsnum
|rsid=9809219
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SDHAP2
|position=251100
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SDHA
}}{{omim
|id=600857
|rsnum=9809219
|variant=0001
}}{{ClinVar
|rsid=9809219
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=251215
|CHROM=5
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050260000000000102110100
|GENEINFO=SDHA:6389
|GENE_NAME=SDHA
|GENE_ID=6389
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.251215C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600857.0001
|CLNSIG=5
|CLNCUI=C1850597
|CLNDBN=Leigh syndrome due to mitochondrial complex II deficiency
|Disease=Leigh syndrome due to mitochondrial complex II deficiency
|CLNACC=RCV000009281.1
|Tags=PM;S3D;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1850597
}}