ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.1103+18C>T

gnomAD frequency: 0.48279  dbSNP: rs438464
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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 RCV000252637 SCV000316775 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701827 SCV001933521 benign Congenital heart defects, multiple types, 7 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701979 SCV001933522 benign Hereditary lymphedema type I 2021-08-10 criteria provided, single submitter clinical testing
GeneDx RCV001709562 SCV001938040 benign not provided 2018-11-11 criteria provided, single submitter clinical testing

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