ClinVar Miner

List of variants in gene RAD9B studied for central nervous system malformation

Included ClinVar conditions (163):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_001286535.2(RAD9B):c.1199dup (p.Arg401fs) rs748778907 0.00004
NM_001286535.2(RAD9B):c.28A>G (p.Ser10Gly) rs372056091 0.00003
NC_000012.11:g.110950633C>G
NM_001286535.2(RAD9B):c.1060A>G (p.Ser354Gly) rs747100389
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
NM_001286535.2(RAD9B):c.960del (p.Ala321fs) rs778121031

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