ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.518-6C>T

gnomAD frequency: 0.00001  dbSNP: rs754270867
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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 RCV002142054 SCV002413051 likely benign Multiple gastrointestinal atresias 2023-07-19 criteria provided, single submitter clinical testing

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