ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.66G>T (p.Leu22=)

dbSNP: rs1337924090
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001473373 SCV001677526 likely benign Glycine encephalopathy 2024-04-02 criteria provided, single submitter clinical testing
Natera, Inc. RCV001473373 SCV002078209 likely benign Glycine encephalopathy 2021-09-01 no assertion criteria provided clinical testing

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