ClinVar Miner

Submissions for variant F8, 23-BP DEL, FS

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000010874 SCV000031101 pathogenic Hereditary factor VIII deficiency disease 1991-08-15 no assertion criteria provided literature only

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