{{Rsnum
|rsid=80338847
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SDHD
|position=112094906
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SDHD
}}{{omim
|id=602690
|rsnum=80338847
|variant=0016
}}{{ClinVar
|rsid=80338847
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=111965630
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=SDHD:6392
|GENE_NAME=SDHD
|GENE_ID=6392
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.111965630T>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1548; 602690.0016
|CLNSIG=5
|CLNCUI=C1868633; C1708353; C0268151
|CLNDBN=Paragangliomas 1; Hereditary Paraganglioma-Pheochromocytoma Syndromes
|Disease=Paragangliomas 1; Hereditary Paraganglioma-Pheochromocytoma Syndromes
|CLNACC=RCV000007316.1; RCV000020523.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen
|CLNDSDBID=NBK1548:C1868633:168000:29072; NBK1548:C1708353
}}{{PMID Auto
|PMID=11391798
|Title=Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.
}}

{{PMID Auto
|PMID=12114404
|Title=Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma.
}}