ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.3220-29A>G

gnomAD frequency: 0.76189  dbSNP: rs659268
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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 RCV000249778 SCV000316809 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001689952 SCV001908467 benign not provided 2018-11-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702411 SCV001933502 benign Congenital heart defects, multiple types, 7 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702410 SCV001933503 benign Hereditary lymphedema type I 2021-08-10 criteria provided, single submitter clinical testing

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