{{Rsnum
|rsid=1061517
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SDHA
|position=218356
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CCDC127,SDHA
}}{{omim
|id=600857
|rsnum=1061517
|variant=0003
}}

{{ClinVar
|rsid=1061517
|Reversed=0
|FwdREF=A
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=218471
|CHROM=5
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x050060000000000102110100
|GENEINFO=CCDC127:133957; SDHA:6389
|GENE_NAME=CCDC127; SDHA
|GENE_ID=133957; 6389
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.218471A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600857.0003
|CLNSIG=5
|CLNCUI=C1850597
|CLNDBN=Leigh syndrome due to mitochondrial complex II deficiency
|Disease=Leigh syndrome due to mitochondrial complex II deficiency
|CLNACC=RCV000009283.2
|Tags=PM;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1850597
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}