{{Rsnum
|rsid=111430410
|Gene=SDHB
|Chromosome=1
|position=17053988
|Orientation=plus
|GMAF=0.0004591
|Gene_s=SDHB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|rsid=111430410
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=17053988
|CHROM=1
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000a05040116100100
|GENEINFO=SDHB:6390
|GENE_NAME=SDHB
|GENE_ID=6390
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.17053988C>T
|CLNSRC=ClinVar; LabCorp
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Pheochromocytoma
|Disease=Pheochromocytoma
|Tags=PM;PMC;SLO;NSM;REF;ASP;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9995; 0.0004591
|CLNACC=RCV000030447.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1548:C0031511:171300:ORPHA29072
|COMMON=0
|CLNSRCID=NM_003000.2:c.32G>A
}}{{PMID|18728283}} Germline SDHB mutations and familial renal cell carcinoma.

{{PMID|19184535}} SDHB-associated renal oncocytoma suggests a broadening of the renal phenotype in hereditary paragangliomatosis.