ClinVar Miner

Submissions for variant NM_001374504.1(TMPRSS6):c.-1-241G>A

gnomAD frequency: 0.37000  dbSNP: rs5756516
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000314826 SCV000483991 benign Microcytic anemia 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004713929 SCV005277227 benign not provided criteria provided, single submitter not provided

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