{{Rsnum
|rsid=137853259
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PDHA1
|position=19355713
|Gene_s=PDHA1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300502
|variant=0022
|rsnum=137853259
}}{{ClinVar
|rsid=137853259
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=19373831
|CHROM=X
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PDHA1:5160
|GENE_NAME=PDHA1
|GENE_ID=5160
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.19373831C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300502.0022
|CLNSIG=5
|CLNCUI=C1839885
|CLNDBN=X-linked Leigh syndrome
|Disease=X-linked Leigh syndrome
|CLNACC=RCV000011639.8
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1839885:308930:506
}}