ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.3437G>A (p.Arg1146His)

gnomAD frequency: 0.07081  dbSNP: rs1130379
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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 RCV000241743 SCV000316810 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001651286 SCV001865119 benign not provided 2021-06-09 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000241743 SCV001921081 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000241743 SCV001959714 benign not specified no assertion criteria provided clinical testing

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