ClinVar Miner

Submissions for variant NM_000132.3(F8):c.1508G>A (p.Arg503His) (rs35383156)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000991025 SCV000482101 likely benign Hereditary factor VIII deficiency disease 2017-04-28 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). Publications were found based on this search. The evidence from the literature, in combination with allele frequency data from public databases where available, was sufficient to determine this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.
Invitae RCV000861315 SCV001001590 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Mendelics RCV000991025 SCV001142127 benign Hereditary factor VIII deficiency disease 2019-05-28 criteria provided, single submitter clinical testing

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