ClinVar Miner

Submissions for variant NM_001197104.2(KMT2A):c.9904G>A (p.Ala3302Thr)

gnomAD frequency: 0.00004  dbSNP: rs551471898
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000979255 SCV001127195 likely benign not provided 2025-01-06 criteria provided, single submitter clinical testing
GeneDx RCV000979255 SCV001916725 benign not provided 2021-04-26 criteria provided, single submitter clinical testing

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