{{Rsnum
|rsid=11203289
|Gene=SDHB
|Chromosome=1
|position=17054012
|Orientation=minus
|GMAF=0.008724
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=SDHB
}}{{omim
|id=185470
|rsnum=11203289
|variant=0014
}}

{{ClinVar
|rsid=11203289
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=17054012
|CHROM=1
|GMAF=0.0087
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x050160000a05050516110100
|GENEINFO=SDHB:6390
|GENE_NAME=SDHB
|GENE_ID=6390
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.17054012G>C
|CLNSRC=Ambry Genetics; ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=a0571; NM_003000.2:c.8C>G; 185470.0014
|CLNSIG=5
|CLNCUI=C2676500
|CLNDBN=Cowden-like syndrome; not provided; AllHighlyPenetrant; Neoplastic Syndromes, Hereditary
|Disease=Cowden-like syndrome; not provided; AllHighlyPenetrant; Neoplastic Syndromes
|CLNACC=RCV000013632.16; RCV000034690.1; RCV000121999.1; RCV000128921.1
|Tags=RV;PM;SLO;NSM;REF;ASP;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9913; 0.008724
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=C2676500:612359:ORPHA201; C0027672
|COMMON=1
}}

{{on chip | HumanOmni1Quad}}