ClinVar Miner

Submissions for variant NM_032242.4(PLXNA1):c.1194+17C>T

gnomAD frequency: 0.03970  dbSNP: rs57299665
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 RCV002118101 SCV002404979 benign not provided 2024-12-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002118101 SCV005301657 benign not provided criteria provided, single submitter not provided

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