ClinVar Miner

Submissions for variant NM_003227.4(TFR2):c.727-10G>C

gnomAD frequency: 0.00001  dbSNP: rs1157089802
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002078083 SCV002325917 likely benign Hereditary hemochromatosis 2021-08-08 criteria provided, single submitter clinical testing

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