ClinVar Miner

List of variants reported as likely benign for Glaucoma 3A

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Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_000104.4(CYP1B1):c.1358A>G (p.Asn453Ser) rs1800440 0.11965
NM_000104.4(CYP1B1):c.-1-14C>T rs4987134 0.02460
NM_000104.4(CYP1B1):c.*2371T>C rs9309020 0.02296
NM_000104.4(CYP1B1):c.1328C>G (p.Ala443Gly) rs4986888 0.01612
NM_000104.4(CYP1B1):c.*926A>C rs9341261 0.01416
NM_000104.4(CYP1B1):c.*2158T>C rs112948057 0.01121
NM_000104.4(CYP1B1):c.*2261A>C rs77534033 0.00985
NM_000104.4(CYP1B1):c.685G>A (p.Glu229Lys) rs57865060 0.00478
NM_000104.4(CYP1B1):c.241T>A (p.Tyr81Asn) rs9282671 0.00362
NM_000104.4(CYP1B1):c.*1853G>T rs9341265 0.00338

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