ClinVar Miner

Submissions for variant F8, EX26DEL

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000010799 SCV000031026 pathogenic Hereditary factor VIII deficiency disease 1988-09-01 no assertion criteria provided literature only
OMIM RCV000010806 SCV000031033 pathogenic Hereditary factor VIII deficiency disease 1995-09-15 no assertion criteria provided literature only
OMIM RCV000010817 SCV000031044 pathogenic Hereditary factor VIII deficiency disease 1989-02-01 no assertion criteria provided literature only
OMIM RCV000010836 SCV000031063 pathogenic Hereditary factor VIII deficiency disease 1995-01-01 no assertion criteria provided literature only

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