{{Rsnum
|rsid=80338842
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SDHD
|position=112086910
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SDHD,TIMM8B
}}{{omim
|id=602690
|rsnum=80338842
|variant=0015
}}{{ClinVar
|rsid=80338842
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=111957634
|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.111957634G>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1548; 602690.0015
|CLNSIG=5
|CLNCUI=C1868633; C1708353
|CLNDBN=Paragangliomas 1; Hereditary Paraganglioma-Pheochromocytoma Syndromes
|Disease=Paragangliomas 1; Hereditary Paraganglioma-Pheochromocytoma Syndromes
|CLNACC=RCV000007315.1; RCV000020522.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen
|CLNDSDBID=NBK1548:C1868633:168000:29072; NBK1548:C1708353
}}{{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=12782822
|Title=Hereditary paraganglioma due to the SDHD M1I mutation in a second Chinese family: a founder effect?
}}