ClinVar Miner

Submissions for variant NM_003982.4(SLC7A7):c.895-20C>T

gnomAD frequency: 0.00002  dbSNP: rs376455152
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002115741 SCV002410436 benign Lysinuric protein intolerance 2024-01-04 criteria provided, single submitter clinical testing

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