ClinVar Miner

Submissions for variant NM_000132.3(F8):c.1086G>A (p.Ala362=) (rs1800289)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000506787 SCV000603530 benign not specified 2017-03-06 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000320462 SCV000482102 likely benign Hemophilia A, FVIII Deficiency 2016-06-14 criteria provided, single submitter clinical testing

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