ClinVar Miner

Submissions for variant NM_022041.4(GAN):c.973+9C>G

gnomAD frequency: 0.00001  dbSNP: rs1383717688
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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 RCV002098196 SCV002389570 likely benign Giant axonal neuropathy 1 2023-12-11 criteria provided, single submitter clinical testing

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