ClinVar Miner

Submissions for variant NM_019616.4(F7):c.220A>G (p.Arg74Gly)

dbSNP: rs2142212748
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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 RCV001420375 SCV001622534 likely pathogenic Factor VII deficiency 2021-04-28 criteria provided, single submitter research

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