ClinVar Miner

Submissions for variant NM_001372.4(DNAH9):c.4626G>A (p.Arg1542=)

dbSNP: rs2074381591
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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 RCV003874934 SCV004683535 likely benign not provided 2024-02-12 criteria provided, single submitter clinical testing

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