ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.2356-8G>A

gnomAD frequency: 0.00004  dbSNP: rs376434109
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001497992 SCV001702732 likely benign Multiple gastrointestinal atresias 2023-12-15 criteria provided, single submitter clinical testing

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