ClinVar Miner

List of variants in gene SDHB reported as likely benign for adrenal gland disease

Included ClinVar conditions (125):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP
NM_003000.2(SDHB):c.-139G>T rs114522228
NM_003000.2(SDHB):c.-37T>C rs143031690
NM_003000.2(SDHB):c.113G>A (p.Arg38His) rs143058777
NM_003000.2(SDHB):c.158G>A (p.Gly53Glu) rs34916635
NM_003000.2(SDHB):c.170A>G (p.His57Arg) rs35962811
NM_003000.2(SDHB):c.21C>T (p.Leu7=) rs147815442
NM_003000.2(SDHB):c.24C>T (p.Ser8=) rs148738139
NM_003000.2(SDHB):c.287-26A>G rs201397253
NM_003000.2(SDHB):c.300T>C (p.Ser100=) rs11541235
NM_003000.2(SDHB):c.32G>A (p.Arg11His) rs111430410
NM_003000.2(SDHB):c.33C>T (p.Arg11=) rs146399542
NM_003000.2(SDHB):c.357C>T (p.Thr119=) rs1553177749
NM_003000.2(SDHB):c.424-14_424-9dup rs1064794554
NM_003000.2(SDHB):c.468T>C (p.Tyr156=) rs199718947
NM_003000.2(SDHB):c.480G>A (p.Lys160=) rs1553177683
NM_003000.2(SDHB):c.487T>C (p.Ser163Pro) rs33927012
NM_003000.2(SDHB):c.516G>A (p.Gln172=) rs138937650
NM_003000.2(SDHB):c.541-18_541-8dup rs1553177448
NM_003000.2(SDHB):c.541-6A>G rs1195530396
NM_003000.2(SDHB):c.642+17T>C rs200597595
NM_003000.2(SDHB):c.700C>T (p.Leu234=) rs201728852
NM_003000.2(SDHB):c.72+7C>A rs1553179311
NM_003000.2(SDHB):c.73-10A>C rs376494419
NM_003000.2(SDHB):c.765+13G>A rs115561881
NM_003000.2(SDHB):c.765+8G>A rs1553177265
NM_003000.2(SDHB):c.766-6T>C rs1553176984
NM_003000.2(SDHB):c.816C>G (p.Thr272=) rs1454454086
NM_003000.2(SDHB):c.8C>G (p.Ala3Gly) rs11203289

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