ClinVar Miner

Submissions for variant NM_001089.3(ABCA3):c.873+84dup

dbSNP: rs5815117
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001544284 SCV001763295 benign Interstitial lung disease due to ABCA3 deficiency 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001713015 SCV001938989 benign not provided 2019-08-16 criteria provided, single submitter clinical testing

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