ClinVar Miner

Submissions for variant NM_004698.4(PRPF3):c.1426+8del

dbSNP: rs2525216752
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 RCV002861443 SCV003214677 likely benign not provided 2022-07-12 criteria provided, single submitter clinical testing

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