ClinVar Miner

Submissions for variant NM_176869.3(PPA2):c.442-17T>A

gnomAD frequency: 0.00096  dbSNP: rs575289677
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 RCV002112225 SCV002386832 benign not provided 2025-01-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002112225 SCV005302073 benign not provided criteria provided, single submitter not provided

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