ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.1103+20A>C

dbSNP: rs383985
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243464 SCV000316776 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702408 SCV001933518 benign Congenital heart defects, multiple types, 7 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701828 SCV001933520 benign Hereditary lymphedema type I 2021-08-10 criteria provided, single submitter clinical testing

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