Submissions for variant NM_182925.5(FLT4):c.2670C>G (p.His890Gln)

gnomAD frequency: 0.61446  dbSNP: rs448012

Total submissions: 7

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
PreventionGenetics, part of Exact Sciences	RCV000251871	SCV000316798	benign	not specified		criteria provided, single submitter	clinical testing
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	RCV000251871	SCV000539181	benign	not specified	2016-03-29	criteria provided, single submitter	clinical testing	Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: 62% of total chromosomes in ExAC
GeneDx	RCV001660381	SCV001880962	benign	not provided	2018-11-11	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV001701830	SCV001933510	benign	Congenital heart defects, multiple types, 7	2021-08-10	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV001701923	SCV001933511	benign	Hereditary lymphedema type I	2021-08-10	criteria provided, single submitter	clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV000251871	SCV001742327	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics, Academic Medical Center	RCV000251871	SCV001923326	benign	not specified		no assertion criteria provided	clinical testing