ClinVar Miner

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

dbSNP: rs190250043
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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 RCV002092361 SCV002324701 likely benign Multiple gastrointestinal atresias 2023-11-25 criteria provided, single submitter clinical testing

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