ClinVar Miner

List of variants in gene SDHB reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_003000.3(SDHB):c.287-156A>G rs2746469 0.95477
NM_003000.3(SDHB):c.201-36G>T rs1022580 0.95416
NM_003000.3(SDHB):c.18C>A (p.Ala6=) rs2746462 0.95374
NM_003000.3(SDHB):c.200+104A>G rs12073028 0.57710
NM_003000.3(SDHB):c.73-302G>A rs732679 0.57710
NM_003000.3(SDHB):c.642+325C>T rs2235930 0.51227
NM_003000.3(SDHB):c.540+256A>C rs11203282 0.42590
NM_003000.3(SDHB):c.286+169A>G rs10887990 0.41910
NM_003000.3(SDHB):c.73-111G>A rs9435745 0.41897
NM_003000.3(SDHB):c.642+225A>G rs2647162 0.27391
NM_003000.3(SDHB):c.200+286G>A rs9787230 0.20943
NM_003000.3(SDHB):c.200+33G>A rs2647169 0.10785
NC_000001.11:g.17018618G>C rs2746477 0.10776
NM_003000.3(SDHB):c.765+256C>G rs761420 0.10583
NM_003000.3(SDHB):c.72+174C>G rs2746463 0.10001
NC_000001.11:g.17054463G>A rs2647211 0.09879
NM_003000.3(SDHB):c.73-203A>G rs76861060 0.05046
NM_003000.3(SDHB):c.200+35G>A rs61769190 0.02530
NM_003000.3(SDHB):c.8C>G (p.Ala3Gly) rs11203289 0.01309
NM_003000.3(SDHB):c.487T>C (p.Ser163Pro) rs33927012 0.00921
NM_003000.2(SDHB):c.-139G>T rs114522228 0.00671
NM_003000.3(SDHB):c.24C>T (p.Ser8=) rs148738139 0.00461
NM_003000.3(SDHB):c.423+20T>A rs190139590 0.00179
NM_003000.3(SDHB):c.300T>C (p.Ser100=) rs11541235 0.00157
NM_003000.3(SDHB):c.423+83C>A rs150146676 0.00135
NM_003000.3(SDHB):c.158G>A (p.Gly53Glu) rs34916635 0.00041
NM_003000.3(SDHB):c.541-43C>G rs773251888 0.00004
NM_003000.3(SDHB):c.552C>T (p.Tyr184=) rs202098600 0.00004
NM_003000.3(SDHB):c.*159del rs532333715
NM_003000.3(SDHB):c.424-37TTC[10] rs34261028
NM_003000.3(SDHB):c.424-37TTC[6] rs34261028
NM_003000.3(SDHB):c.424-37TTC[7] rs34261028
NM_003000.3(SDHB):c.540+218C>T rs6696035
NM_003000.3(SDHB):c.642+230T>C rs2746471
NM_003000.3(SDHB):c.72+246_72+247del rs35029966
NM_003000.3(SDHB):c.72+247del rs35029966
NM_003000.3(SDHB):c.766-177dup rs35456786

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