{{Rsnum
|rsid=80338846
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SDHD
|Gene_s=SDHD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=112088981
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000020521.1
|CLNALLE=1
|CLNDBN=Hereditary Paraganglioma-Pheochromocytoma Syndromes
|CLNDSDB=GeneReviews:MedGen
|CLNDSDBID=NBK1548:C1708353
|CLNHGVS=NC_000011.9:g.111959705T>C
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1548
|Disease=Hereditary Paraganglioma-Pheochromocytoma Syndromes
|FwdALT=C
|FwdREF=T
|GENEINFO=SDHD:6392
|GENE_ID=6392
|GENE_NAME=SDHD
|REF=T
|RSPOS=111959705
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=131
|rsid=80338846
}}{{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.
}}