ClinVar Miner

Submissions for variant NM_002133.3(HMOX1):c.784C>T (p.Arg262Cys)

gnomAD frequency: 0.00063  dbSNP: rs149487862
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001348789 SCV001543106 likely benign not provided 2024-12-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001348789 SCV005195391 uncertain significance not provided criteria provided, single submitter not provided

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