ClinVar Miner

Submissions for variant NM_002458.3(MUC5B):c.2769+8G>A

gnomAD frequency: 0.00001  dbSNP: rs771601782
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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 RCV000943407 SCV001089353 likely benign not provided 2018-08-22 criteria provided, single submitter clinical testing

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