ClinVar Miner

Submissions for variant NM_004793.4(LONP1):c.1773+9G>A

gnomAD frequency: 0.00429  dbSNP: rs200985875
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000966472 SCV001113799 benign not provided 2025-01-30 criteria provided, single submitter clinical testing
GeneDx RCV000966472 SCV001780381 likely benign not provided 2020-01-29 criteria provided, single submitter clinical testing

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