ClinVar Miner

Submissions for variant NM_004698.4(PRPF3):c.672C>T (p.Ile224=)

gnomAD frequency: 0.00004  dbSNP: rs376095546
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 RCV002183445 SCV002473940 likely benign not provided 2022-03-10 criteria provided, single submitter clinical testing

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