ClinVar Miner

Submissions for variant NM_006445.4(PRPF8):c.5619+16G>C

gnomAD frequency: 0.00198  dbSNP: rs143752933
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 RCV001512934 SCV001720435 benign not provided 2024-12-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001512934 SCV005249776 benign not provided criteria provided, single submitter not provided

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