ClinVar Miner

Submissions for variant NM_130849.4(SLC39A4):c.193-89A>C

gnomAD frequency: 0.49986  dbSNP: rs2280839
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001543988 SCV001762909 benign Hereditary acrodermatitis enteropathica 2021-07-10 criteria provided, single submitter clinical testing
GeneDx RCV001647393 SCV001859199 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001647393 SCV005269804 benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV001543988 SCV002083135 benign Hereditary acrodermatitis enteropathica 2019-08-26 no assertion criteria provided clinical testing

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