ClinVar Miner

Submissions for variant NM_001242896.3(DEPDC5):c.1936dup (p.Ser646fs)

dbSNP: rs1569012755
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biochemistry Laboratory of CDMU, Chengde Medical University RCV000768449 SCV000899211 pathogenic Epilepsy, familial focal, with variable foci 1 no assertion criteria provided case-control

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