ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.1287+9C>T

gnomAD frequency: 0.00001  dbSNP: rs1677447803
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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 RCV002076904 SCV002325045 likely benign Multiple gastrointestinal atresias 2021-08-09 criteria provided, single submitter clinical testing

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