ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.2479-159T>C

gnomAD frequency: 0.04818  dbSNP: rs79478703
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001693017 SCV001911238 benign not provided 2018-07-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001693017 SCV005239551 benign not provided criteria provided, single submitter not provided

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