ClinVar Miner

Variants in gene SDHB with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 17
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HGVS dbSNP gnomAD frequency
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_003000.3(SDHB):c.24C>T (p.Ser8=) rs148738139 0.00461
NM_003000.3(SDHB):c.-37T>C rs143031690 0.00411
NM_003000.3(SDHB):c.170A>G (p.His57Arg) rs35962811 0.00231
NM_003000.3(SDHB):c.32G>A (p.Arg11His) rs111430410 0.00185
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.21C>T (p.Leu7=) rs147815442 0.00054
NM_003000.3(SDHB):c.158G>A (p.Gly53Glu) rs34916635 0.00041
NM_003000.3(SDHB):c.552C>T (p.Tyr184=) rs202098600 0.00004
NM_003000.3(SDHB):c.765+13G>A rs115561881 0.00002
NM_003000.3(SDHB):c.287-4T>C rs200419171 0.00001
NM_003000.2(SDHB):c.424-16_424-14dup rs34261028
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

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