Submissions for variant NM_000791.4(DHFR):c.-437GGGGCGCTG[3]

dbSNP: rs60484572

Total submissions: 10

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia	RCV000202801	SCV000257918	uncertain significance	not specified	2015-03-25	criteria provided, single submitter	clinical testing
Labcorp Genetics (formerly Invitae), Labcorp	RCV000951258	SCV001097639	benign	not provided	2018-04-10	criteria provided, single submitter	clinical testing
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden	RCV000951258	SCV002010464	likely benign	not provided	2021-11-03	criteria provided, single submitter	clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano	RCV000951258	SCV002046936	benign	not provided	2021-05-07	criteria provided, single submitter	clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	RCV000951258	SCV002048642	benign	not provided	2024-09-13	criteria provided, single submitter	clinical testing
Sema4, Sema4	RCV002256112	SCV002536016	benign	Hereditary cancer-predisposing syndrome	2021-06-18	criteria provided, single submitter	curation
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital	RCV000202801	SCV002570201	benign	not specified	2025-03-04	criteria provided, single submitter	clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center	RCV000202801	SCV001809099	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics, Academic Medical Center	RCV000202801	SCV001923100	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute	RCV000202801	SCV001977628	benign	not specified		no assertion criteria provided	clinical testing