ClinVar Miner

Submissions for variant NM_130849.4(SLC39A4):c.63G>C (p.Thr21=)

gnomAD frequency: 0.04058  dbSNP: rs13251676
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000276651 SCV000472592 likely benign Hereditary acrodermatitis enteropathica 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001516304 SCV001724572 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000276651 SCV001762911 likely benign Hereditary acrodermatitis enteropathica 2021-07-10 criteria provided, single submitter clinical testing
GeneDx RCV001516304 SCV001902226 benign not provided 2021-06-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001516304 SCV005222922 likely benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV000276651 SCV002083139 benign Hereditary acrodermatitis enteropathica 2019-11-22 no assertion criteria provided clinical testing

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