ClinVar Miner

Submissions for variant NM_003665.4(FCN3):c.393+178T>A

gnomAD frequency: 0.68742  dbSNP: rs10794501
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biochemistry and Molecular Biology, Faculty of Pharmacy, Al-Azhar University RCV001280947 SCV001468299 uncertain significance Rheumatic heart disease 2019-01-09 no assertion criteria provided case-control

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