ClinVar Miner

Submissions for variant NM_022552.5(DNMT3A):c.2173+26C>T

gnomAD frequency: 0.41532  dbSNP: rs2289195
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 RCV001619442 SCV001847584 benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001619442 SCV005239584 benign not provided criteria provided, single submitter not provided

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