ClinVar Miner

Submissions for variant NM_012144.4(DNAI1):c.1401+7A>G

gnomAD frequency: 0.00017  dbSNP: rs370745702
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001510327 SCV001717337 benign Primary ciliary dyskinesia 2024-07-17 criteria provided, single submitter clinical testing

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