ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.640-1663G>A

gnomAD frequency: 0.68029  dbSNP: rs11681447
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001719458 SCV001948692 benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001719458 SCV005239684 benign not provided criteria provided, single submitter not provided

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