{{Rsnum
|rsid=34677591
|Gene=SDHD
|Chromosome=11
|position=112086941
|Orientation=plus
|GMAF=0.005969
|Gene_s=SDHD,TIMM8B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{omim
|id=602690
|rsnum=34677591
|variant=0011
}}

{{ClinVar
|rsid=34677591
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=111957665
|CHROM=11
|GMAF=0.006
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050060000000040516110100
|GENEINFO=SDHD:6392; TIMM8B:26521
|GENE_NAME=SDHD; TIMM8B
|GENE_ID=6392; 26521
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.111957665G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602690.0011
|CLNSIG=5
|CLNCUI=C2676500; C1868633; C0349535; C0031511
|CLNDBN=Cowden disease 3; Paragangliomas 1; Carcinoid tumor of intestine; Pheochromocytoma; not provided
|Disease=Cowden disease 3; Paragangliomas 1; Carcinoid tumor of intestine; Pheochromocytoma; not provided
|CLNACC=RCV000007299.1; RCV000007300.1; RCV000007301.1; RCV000007302.1; RCV000034697.1
|Tags=PM;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.994; 0.005969
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:SNOMED_CT
|CLNDSDBID=CN166604:615106:201; NBK1548:C1868633:168000:29072; C0349535:114900:276816003; NBK1548:C0031511:171300:29072
|COMMON=1
}}

{{GET Evidence
|gene=SDHD
|aa_change=Gly12Ser
|aa_change_short=G12S
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs34677591
|overall_frequency_n=87
|overall_frequency_d=10758
|overall_frequency=0.008087
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|in_omim=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=2
|autoscore=5
|webscore=N
|n_web_uneval=10
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}