ClinVar Miner

Submissions for variant NM_014727.3(KMT2B):c.4303-13C>T

gnomAD frequency: 0.00238  dbSNP: rs73590580
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001565345 SCV001788677 likely benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001565345 SCV002356816 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001565345 SCV005206999 likely benign not provided criteria provided, single submitter not provided

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