ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.2761+44G>A

gnomAD frequency: 0.66129  dbSNP: rs446003
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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 RCV000244254 SCV000316799 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001594924 SCV001829075 benign not provided 2018-11-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701981 SCV001933506 benign Congenital heart defects, multiple types, 7 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701924 SCV001933509 benign Hereditary lymphedema type I 2021-08-10 criteria provided, single submitter clinical testing

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