ClinVar Miner

Submissions for variant NM_000341.4(SLC3A1):c.1012-23C>T

gnomAD frequency: 0.00284  dbSNP: rs201121824
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 RCV002195646 SCV002490703 benign Cystinuria 2024-12-12 criteria provided, single submitter clinical testing

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