ClinVar Miner

List of variants in gene SDHB reported as likely pathogenic for cardiovascular organ benign neoplasm

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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NM_003000.2(SDHB):c.131_139del (p.Ile44_Trp47delinsArg) rs864321639
NM_003000.2(SDHB):c.143A>T (p.Asp48Val) rs202101384
NM_003000.2(SDHB):c.1A>T (p.Met1Leu) rs1131691049
NM_003000.2(SDHB):c.201-2A>C rs878854574
NM_003000.2(SDHB):c.227T>G (p.Leu76Ter) rs864321638
NM_003000.2(SDHB):c.251A>C (p.Asp84Ala) rs864321637
NM_003000.2(SDHB):c.286G>A (p.Gly96Ser) rs587782243
NM_003000.2(SDHB):c.338G>C (p.Cys113Ser) rs864321636
NM_003000.2(SDHB):c.590C>G (p.Pro197Arg) rs74315367
NM_003000.2(SDHB):c.598T>C (p.Trp200Arg) rs1557739966
NM_003000.2(SDHB):c.649C>T (p.Arg217Cys) rs200245469
NM_003000.2(SDHB):c.724C>A (p.Arg242Ser) rs786203251
NM_003000.2(SDHB):c.780dup (p.Lys261fs) rs1557738304
NM_003000.2(SDHB):c.784_787dup (p.Ile263fs) rs1553176976
NM_003000.2(SDHB):c.785_786insG (p.Ile263fs) rs1553176979

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