Submissions for variant NM_000371.3(TTR):c.337-18G>C (rs36204272)

Total submissions: 9

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	RCV000030574	SCV000053249	benign	Cardiomyopathy	2011-08-18	criteria provided, single submitter	curation	Converted during submission to Benign.
PreventionGenetics,PreventionGenetics	RCV000248110	SCV000303886	benign	not specified	2016-04-04	criteria provided, single submitter	clinical testing
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics	RCV000248110	SCV000332774	benign	not specified	2015-07-06	criteria provided, single submitter	clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories	RCV001283523	SCV001157234	benign	none provided	2020-09-01	criteria provided, single submitter	clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre	RCV001173542	SCV001336632	benign	Charcot-Marie-Tooth disease		criteria provided, single submitter	clinical testing
GeneDx	RCV001711094	SCV001940488	benign	not provided	2015-03-03	criteria provided, single submitter	clinical testing
Clinical Genetics,Academic Medical Center	RCV000248110	SCV001922686	benign	not specified		no assertion criteria provided	clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht	RCV000248110	SCV001932568	benign	not specified		no assertion criteria provided	clinical testing
Human Genetics - Radboudumc,Radboudumc	RCV000248110	SCV001952480	benign	not specified		no assertion criteria provided	clinical testing