ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.1392+9G>T

gnomAD frequency: 0.00013  dbSNP: rs368491762
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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 RCV001441470 SCV001644401 likely benign Multiple gastrointestinal atresias 2022-08-31 criteria provided, single submitter clinical testing

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