ClinVar Miner

Submissions for variant NM_030943.4(AMN):c.1089C>T (p.Gly363=)

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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 RCV003505850 SCV004368208 likely benign Imerslund-Grasbeck syndrome 2023-12-19 criteria provided, single submitter clinical testing

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