ClinVar Miner

Submissions for variant NM_000132.4(F8):c.266-19G>A

gnomAD frequency: 0.00623  dbSNP: rs28370201
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000991028 SCV001142130 benign Hereditary factor VIII deficiency disease 2019-05-28 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003656659 SCV001471981 benign not provided 2023-11-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV003656659 SCV005276570 benign not provided criteria provided, single submitter not provided

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