ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.348+12G>A

gnomAD frequency: 0.00005  dbSNP: rs777847973
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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 RCV002132272 SCV002404255 benign Multiple gastrointestinal atresias 2024-07-09 criteria provided, single submitter clinical testing

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