ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.1080G>T (p.Val360=)

gnomAD frequency: 0.00001  dbSNP: rs745502236
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000954538 SCV001101175 likely benign Glycine encephalopathy 2024-12-09 criteria provided, single submitter clinical testing

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