ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.2168-49G>A

gnomAD frequency: 0.23522  dbSNP: rs2242214
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241557 SCV000316793 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702409 SCV001933514 benign Congenital heart defects, multiple types, 7 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701920 SCV001933515 benign Hereditary lymphedema type I 2021-08-10 criteria provided, single submitter clinical testing
GeneDx RCV001711751 SCV001942469 benign not provided 2018-11-11 criteria provided, single submitter clinical testing

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