ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.4512C>T (p.Val1504=)

gnomAD frequency: 0.03041  dbSNP: rs17013240
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000948141 SCV001094337 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV000948141 SCV001835779 benign not provided 2018-07-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000948141 SCV005275888 benign not provided criteria provided, single submitter not provided

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