ClinVar Miner

Submissions for variant NM_001270974.2(HYDIN):c.9249-13T>A

dbSNP: rs1798454
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital RCV001733559 SCV001984163 likely benign Primary ciliary dyskinesia 5 2020-03-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706247 SCV005219115 likely benign not provided criteria provided, single submitter not provided

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