ClinVar Miner

Submissions for variant NM_033419.5(PGAP3):c.280-209C>G

gnomAD frequency: 0.51546  dbSNP: rs2517953
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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 RCV001598122 SCV001830479 benign not provided 2018-07-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001598122 SCV005247473 benign not provided criteria provided, single submitter not provided

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