ClinVar Miner

Submissions for variant NM_006445.4(PRPF8):c.5943G>A (p.Val1981=)

dbSNP: rs758937794
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001436964 SCV001639810 likely benign not provided 2025-01-13 criteria provided, single submitter clinical testing

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