ClinVar Miner

Submissions for variant NM_130849.4(SLC39A4):c.1114= (p.Val372=)

gnomAD frequency: 0.24978  dbSNP: rs1871534
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000393204 SCV000472566 benign Hereditary acrodermatitis enteropathica 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001515871 SCV001724040 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001515871 SCV005269797 benign not provided criteria provided, single submitter not provided

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