ClinVar Miner

Submissions for variant NM_002458.3(MUC5B):c.2725G>A (p.Asp909Asn)

gnomAD frequency: 0.00017  dbSNP: rs80298911
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001332134 SCV001524352 uncertain significance Interstitial lung disease 2 2020-03-20 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Fulgent Genetics, Fulgent Genetics RCV001332134 SCV002783756 uncertain significance Interstitial lung disease 2 2022-01-31 criteria provided, single submitter clinical testing

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