ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.448+118G>C

dbSNP: rs114783583
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001708121 SCV001935685 benign not provided 2018-07-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001708121 SCV005241882 benign not provided criteria provided, single submitter not provided

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