ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.2018-19G>T

dbSNP: rs143365344
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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 RCV001516854 SCV001725213 benign Multiple gastrointestinal atresias 2025-01-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004709053 SCV005241278 benign not provided criteria provided, single submitter not provided

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