ClinVar Miner

Submissions for variant NM_014270.5(SLC7A9):c.201C>T (p.Ile67=)

gnomAD frequency: 0.00002  dbSNP: rs371635071
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000762003 SCV000892238 uncertain significance not provided 2018-08-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000762003 SCV001639782 likely benign not provided 2022-07-11 criteria provided, single submitter clinical testing

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