ClinVar Miner

Submissions for variant NM_022041.4(GAN):c.852-8T>C

gnomAD frequency: 0.00001  dbSNP: rs780786555
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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 RCV000525612 SCV000640443 likely benign Giant axonal neuropathy 1 2020-02-07 criteria provided, single submitter clinical testing

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