{{Rsnum
|rsid=80338843
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SDHD
|position=112087916
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SDHD,TIMM8B
}}{{omim
|id=602690
|rsnum=80338843
|variant=0002
}}{{ClinVar
|rsid=80338843
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=111958640
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=SDHD:6392; TIMM8B:26521
|GENE_NAME=SDHD; TIMM8B
|GENE_ID=6392; 26521
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.111958640C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1548; 602690.0002
|CLNSIG=5
|CLNCUI=C1868633; C0031511; C1708353
|CLNDBN=Paragangliomas 1; Pheochromocytoma; Hereditary Paraganglioma-Pheochromocytoma Syndromes
|Disease=Paragangliomas 1; Pheochromocytoma; Hereditary Paraganglioma-Pheochromocytoma Syndromes
|CLNACC=RCV000007296.1; RCV000007297.1; RCV000020518.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen
|CLNDSDBID=NBK1548:C1868633:168000:29072; NBK1548:C0031511:171300:29072; NBK1548:C1708353
}}{{PMID Auto
|PMID=10657297
|Title=Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
}}

{{PMID Auto
|PMID=11156372
|Title=Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma.
}}

{{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=11897817
|Title=Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.
|OA=1
}}