ClinVar Miner

Submissions for variant NM_130849.4(SLC39A4):c.-21T>G

gnomAD frequency: 0.01680  dbSNP: rs77422016
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000372301 SCV000472594 benign Hereditary acrodermatitis enteropathica 2016-06-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000372301 SCV001762912 benign Hereditary acrodermatitis enteropathica 2021-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004712534 SCV005269808 benign not provided criteria provided, single submitter not provided

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