Submissions for variant NM_181882.3(PRX):c.4059GGA[6] (p.Glu1361del)

dbSNP: rs139624657

Total submissions: 12

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Labcorp Genetics (formerly Invitae), Labcorp	RCV000200304	SCV000252891	benign	Charcot-Marie-Tooth disease type 4	2025-02-03	criteria provided, single submitter	clinical testing
Eurofins Ntd Llc (ga)	RCV000344573	SCV000333751	benign	not specified	2015-08-13	criteria provided, single submitter	clinical testing
Athena Diagnostics	RCV000576819	SCV000677435	benign	Charcot-Marie-Tooth disease type 4F	2017-05-24	criteria provided, single submitter	clinical testing
Mendelics	RCV000990214	SCV001141084	benign	Spinocerebellar ataxia 46	2019-05-28	criteria provided, single submitter	clinical testing
Molecular Genetics Laboratory, London Health Sciences Centre	RCV000857043	SCV001337084	benign	Charcot-Marie-Tooth disease		criteria provided, single submitter	clinical testing
GeneDx	RCV001706183	SCV001904925	benign	not provided	2015-03-03	criteria provided, single submitter	clinical testing
Genesis Genome Database	RCV000857043	SCV000999613	uncertain significance	Charcot-Marie-Tooth disease	2019-08-14	no assertion criteria provided	research
Genesis Genome Database	RCV000857044	SCV000999614	uncertain significance	Charcot-Marie-Tooth disease, type I	2019-08-14	no assertion criteria provided	research
Genesis Genome Database	RCV000857045	SCV000999615	uncertain significance	Charcot-Marie-Tooth disease type 5	2019-08-14	no assertion criteria provided	research
Genesis Genome Database	RCV000200304	SCV000999616	uncertain significance	Charcot-Marie-Tooth disease type 4	2019-08-14	no assertion criteria provided	research
Clinical Genetics, Academic Medical Center	RCV000344573	SCV001917001	benign	not specified		no assertion criteria provided	clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV000344573	SCV001963016	benign	not specified		no assertion criteria provided	clinical testing