ClinVar Miner

Submissions for variant NM_004977.3(KCNC3):c.1017C>T (p.Asn339=)

gnomAD frequency: 0.00003  dbSNP: rs371799397
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000905023 SCV001049581 likely benign not provided 2024-11-27 criteria provided, single submitter clinical testing
Athena Diagnostics RCV001664540 SCV001879953 benign not specified 2021-06-07 criteria provided, single submitter clinical testing

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