ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.648+20G>A

gnomAD frequency: 0.00014  dbSNP: rs200822853
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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 RCV002164695 SCV002333366 benign Multiple gastrointestinal atresias 2024-10-30 criteria provided, single submitter clinical testing

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