ClinVar Miner

Submissions for variant NM_181776.3(SLC36A2):c.1181-5T>C

gnomAD frequency: 0.00017  dbSNP: rs190486100
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 RCV000903188 SCV001047644 benign not provided 2024-07-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495462 SCV002799867 likely benign Hyperglycinuria; Iminoglycinuria 2021-08-17 criteria provided, single submitter clinical testing

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