ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.348+7C>A

dbSNP: rs553269542
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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 RCV001497447 SCV001702174 likely benign Multiple gastrointestinal atresias 2021-09-21 criteria provided, single submitter clinical testing

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