{{Rsnum
|rsid=80338844
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SDHD
|position=112088939
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SDHD
}}{{omim
|id=602690
|rsnum=80338844
|variant=0003
}}{{ClinVar
|rsid=80338844
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=111959663
|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.111959663C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1548; 602690.0003
|CLNSIG=255
|CLNCUI=C1868633; C1708353
|CLNDBN=Paragangliomas 1; Pheochromocytoma, somatic; Hereditary Paraganglioma-Pheochromocytoma Syndromes; PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS
|Disease=Paragangliomas 1; Pheochromocytoma; Hereditary Paraganglioma-Pheochromocytoma Syndromes; PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS
|CLNACC=RCV000007303.1; RCV000007304.1; RCV000020519.1; RCV000023206.1
|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=11391
|Title=The estimation of pancreatic lipase--a brief review.
}}

{{PMID Auto
|PMID=10657297
|Title=Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
}}

{{PMID Auto
|PMID=11343322
|Title=Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma.
}}

{{PMID Auto
|PMID=11391796
|Title=Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss.
}}

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

{{PMID Auto
|PMID=12811540
|Title=Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect.
}}