ClinVar Miner

Submissions for variant NM_002458.3(MUC5B):c.2316C>T (p.Ala772=)

gnomAD frequency: 0.00005  dbSNP: rs767758324
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000919457 SCV001064803 likely benign not provided 2018-05-25 criteria provided, single submitter clinical testing

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