ClinVar Miner

Submissions for variant NM_001320.7(CSNK2B):c.577del (p.His193fs)

dbSNP: rs1802056827
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV001280794 SCV001468120 uncertain significance not provided 2020-10-05 criteria provided, single submitter clinical testing

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