ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.334+16_334+22del

dbSNP: rs1819700494
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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 RCV002216967 SCV002367580 likely benign Glycine encephalopathy 2023-05-25 criteria provided, single submitter clinical testing

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