ClinVar Miner

Submissions for variant NM_000132.3(F8):c.4500G>A (p.Pro1500=) (rs33921347)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000756125 SCV000883844 benign not provided 2017-09-22 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000314352 SCV000482093 likely benign Hemophilia A, FVIII Deficiency 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000246522 SCV000302443 benign not specified criteria provided, single submitter clinical testing

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