ClinVar Miner

Submissions for variant NM_182925.5(FLT4):c.3460G>A (p.Gly1154Arg)

gnomAD frequency: 0.00541  dbSNP: rs75614493
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000871008 SCV001012599 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000871008 SCV002048430 likely benign not provided 2020-10-25 criteria provided, single submitter clinical testing

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