ClinVar Miner

Submissions for variant NM_022114.4(PRDM16):c.2940-36G>T

dbSNP: rs41303861
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001719638 SCV001948905 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001789560 SCV002031825 benign Left ventricular noncompaction 8 2021-10-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001719638 SCV005284468 benign not provided criteria provided, single submitter not provided

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