ClinVar Miner

Submissions for variant NM_002662.5(PLD1):c.666-196C>T

gnomAD frequency: 0.13457  dbSNP: rs9882641
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 RCV001684073 SCV001898860 benign not provided 2021-05-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001684073 SCV005306317 benign not provided criteria provided, single submitter not provided

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