ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.27C>T (p.Pro9=)

gnomAD frequency: 0.08237  dbSNP: rs41284843
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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 RCV001521675 SCV001731061 benign Tatton-Brown-Rahman overgrowth syndrome 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001724335 SCV001949588 benign not provided 2018-07-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001724335 SCV005241904 benign not provided criteria provided, single submitter not provided

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