ClinVar Miner

Submissions for variant NM_001994.3(F13B):c.881A>T (p.His294Leu)

dbSNP: rs2125068412
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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 RCV001420397 SCV001622457 uncertain significance Factor XIII, b subunit, deficiency of 2021-04-28 criteria provided, single submitter research

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