ClinVar Miner

Submissions for variant NM_000824.5(GLRB):c.751+13C>G

dbSNP: rs1344006346
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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 RCV003039191 SCV003333362 likely benign Hyperekplexia 2 2024-06-22 criteria provided, single submitter clinical testing

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