ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.2356-9C>T

gnomAD frequency: 0.00003  dbSNP: rs373276280
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001473018 SCV001677162 likely benign Multiple gastrointestinal atresias 2024-10-22 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003900631 SCV004709124 likely benign TTC7A-related disorder 2022-04-26 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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