ClinVar Miner

Submissions for variant NM_022042.4(SLC26A1):c.315C>G (p.Ser105=)

gnomAD frequency: 0.00014  dbSNP: rs377636525
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 RCV002144809 SCV002420768 likely benign not provided 2024-01-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500087 SCV002806699 likely benign Calcium oxalate urolithiasis 2021-11-30 criteria provided, single submitter clinical testing

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