ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.2017+8C>T

gnomAD frequency: 0.00003  dbSNP: rs367595962
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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 RCV000891339 SCV001035151 likely benign Multiple gastrointestinal atresias 2022-09-01 criteria provided, single submitter clinical testing

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