ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.2574C>T (p.Leu858=)

dbSNP: rs2103677768
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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 RCV002139775 SCV002445666 likely benign Multiple gastrointestinal atresias 2022-07-05 criteria provided, single submitter clinical testing

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