ClinVar Miner

Submissions for variant NM_173653.4(SLC9A9):c.707T>C (p.Leu236Ser)

gnomAD frequency: 0.00362  dbSNP: rs113649536
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000893642 SCV001037595 benign not provided 2019-01-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000893642 SCV005303051 benign not provided criteria provided, single submitter not provided
CeGaT Center for Human Genetics Tuebingen RCV000893642 SCV005909980 likely benign not provided 2025-03-01 criteria provided, single submitter clinical testing SLC9A9: BS1

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