Submissions for variant NM_130849.4(SLC39A4):c.340G>A (p.Ala114Thr)

gnomAD frequency: 0.43910  dbSNP: rs17855765

Total submissions: 7

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Illumina Laboratory Services, Illumina	RCV000359976	SCV000472585	benign	Hereditary acrodermatitis enteropathica	2016-06-14	criteria provided, single submitter	clinical testing
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	RCV000455765	SCV000540373	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: Frequency
Labcorp Genetics (formerly Invitae), Labcorp	RCV001515873	SCV001724042	benign	not provided	2024-02-01	criteria provided, single submitter	clinical testing
Genome-Nilou Lab	RCV000359976	SCV001762907	benign	Hereditary acrodermatitis enteropathica	2021-07-10	criteria provided, single submitter	clinical testing
GeneDx	RCV001515873	SCV001900807	benign	not provided	2021-06-09	criteria provided, single submitter	clinical testing
Breakthrough Genomics, Breakthrough Genomics	RCV001515873	SCV005269802	benign	not provided		criteria provided, single submitter	not provided
Natera, Inc.	RCV000359976	SCV001452042	benign	Hereditary acrodermatitis enteropathica	2020-09-16	no assertion criteria provided	clinical testing