ClinVar Miner

Submissions for variant NM_130849.4(SLC39A4):c.10C>T (p.Leu4=)

gnomAD frequency: 0.00288  dbSNP: rs144946747
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000970195 SCV001117762 benign not provided 2024-01-30 criteria provided, single submitter clinical testing
Natera, Inc. RCV001273726 SCV001457109 benign Hereditary acrodermatitis enteropathica 2020-09-16 no assertion criteria provided clinical testing

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