ClinVar Miner

Submissions for variant NM_001032382.2(PQBP1):c.577+25G>A

gnomAD frequency: 0.00512  dbSNP: rs142702270
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001564328 SCV001787478 likely benign not provided 2019-01-13 criteria provided, single submitter clinical testing

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