ClinVar Miner

List of variants reported as likely pathogenic by Finnell Lab,Baylor College of Medicine

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ClinVar version:
Total variants: 6
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HGVS dbSNP
NC_000012.11:g.110950633C>G
NM_001286535.2(RAD9B):c.1060A>G (p.Ser354Gly) rs747100389
NM_001286535.2(RAD9B):c.28A>G (p.Ser10Gly) rs372056091
NM_001286535.2(RAD9B):c.336A>G (p.Ile112Met) rs1593037878
NM_001286535.2(RAD9B):c.645T>A (p.Phe215Leu) rs1593083585
NM_001286535.2(RAD9B):c.661G>A (p.Gly221Arg) rs763079713

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