ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.640-3791G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003407175 SCV004138699 benign not provided 2022-04-01 criteria provided, single submitter clinical testing DNMT3A: BS1, BS2

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