ClinVar Miner

Submissions for variant NM_001384125.1(BLTP1):c.9389-27del

dbSNP: rs10718670
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
GeneDx RCV001686931 SCV001904968 benign not provided 2021-05-13 criteria provided, single submitter clinical testing

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