ClinVar Miner

Submissions for variant NM_006766.5(KAT6A):c.4707C>T (p.Tyr1569=)

gnomAD frequency: 0.00009  dbSNP: rs144938298
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
GeneDx RCV001660797 SCV001873146 benign not provided 2020-12-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001660797 SCV003781093 benign not provided 2023-06-03 criteria provided, single submitter clinical testing

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