ClinVar Miner

Submissions for variant NM_000129.3(F13A1):c.1817del (p.His606fs) (rs1561641262)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Genetics,Necip Fazıl Sehir Hastanesi RCV000754780 SCV000864260 pathogenic Factor XIII, A subunit, deficiency of no assertion criteria provided clinical testing

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