ClinVar Miner

Submissions for variant NM_001323289.2(CDKL5):c.978-23T>C

gnomAD frequency: 0.00005  dbSNP: rs267608555
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
RettBASE RCV000144142 SCV000189219 not provided not provided flagged submission not provided
RettBASE RCV000169972 SCV000222275 benign not specified 2014-05-09 no assertion criteria provided curation

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