{{Rsnum
|rsid=137852768
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SDHA
|position=251338
|Gene_s=SDHA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600857
|variant=0004
|rsnum=137852768
}}{{ClinVar
|rsid=137852768
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=251453
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SDHA:6389
|GENE_NAME=SDHA
|GENE_ID=6389
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.251453G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600857.0004
|CLNSIG=5
|CLNCUI=C1855008; C0023264; C3150898
|CLNDBN=Mitochondrial complex II deficiency; Leigh's disease; Dilated cardiomyopathy 1GG
|Disease=Mitochondrial complex II deficiency; Leigh's disease; Dilated cardiomyopathy 1GG
|CLNACC=RCV000009284.1; RCV000009285.1; RCV000009286.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM; GeneReviews:GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=C1855008:252011; NBK1173:NBK1203:NBK1224:C0023264:256000:ORPHA506:29570005; C3150898:613642:154
}}