ClinVar Miner

Submissions for variant NM_000130.5(F5):c.3995T>C (p.Leu1332Pro)

dbSNP: rs1241060030
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV001420389 SCV001622449 uncertain significance Factor V deficiency 2021-04-28 criteria provided, single submitter research
Revvity Omics, Revvity RCV003145661 SCV003832325 uncertain significance not provided 2021-12-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV003145661 SCV005187043 uncertain significance not provided criteria provided, single submitter not provided

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