ClinVar Miner

Submissions for variant NM_001197104.2(KMT2A):c.10092C>T (p.His3364=)

gnomAD frequency: 0.00019  dbSNP: rs782320299
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 RCV000973251 SCV001120993 likely benign not provided 2023-12-07 criteria provided, single submitter clinical testing
GeneDx RCV000973251 SCV001902512 benign not provided 2019-04-18 criteria provided, single submitter clinical testing

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