ClinVar Miner

Submissions for variant NM_021175.4(HAMP):c.150+15G>A

gnomAD frequency: 0.00001  dbSNP: rs769666853
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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 RCV003750473 SCV004510220 likely benign Hereditary hemochromatosis 2024-03-17 criteria provided, single submitter clinical testing

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