ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.1104-42T>C

gnomAD frequency: 0.94231  dbSNP: rs402647
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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 RCV000243353 SCV000316779 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001636838 SCV001847859 benign not provided 2018-11-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701829 SCV001933516 benign Congenital heart defects, multiple types, 7 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701980 SCV001933517 benign Hereditary lymphedema type I 2021-08-10 criteria provided, single submitter clinical testing

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