ClinVar Miner

Submissions for variant F8, EX5DEL

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000010848 SCV000031075 pathogenic Hereditary factor VIII deficiency disease 1990-01-01 no assertion criteria provided literature only
OMIM RCV000010849 SCV000031076 pathogenic Hereditary factor VIII deficiency disease 1990-01-01 no assertion criteria provided literature only

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