ClinVar Miner

Submissions for variant NM_001372.4(DNAH9):c.4599G>A (p.Arg1533=)

dbSNP: rs2150753781
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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 RCV002144225 SCV002466630 likely benign not provided 2021-04-14 criteria provided, single submitter clinical testing

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