ClinVar Miner

Submissions for variant NM_019616.4(F7):c.394G>T (p.Glu132Ter)

dbSNP: rs146795869
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Total submissions: 1
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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 RCV001420377 SCV001622536 pathogenic Factor VII deficiency 2021-04-28 criteria provided, single submitter research

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