ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.1335C>T (p.Pro445=)

gnomAD frequency: 0.00001  dbSNP: rs1678029487
Minimum review status: Collection method:
Minimum conflict level:
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 RCV002208583 SCV002491803 likely benign Multiple gastrointestinal atresias 2023-06-16 criteria provided, single submitter clinical testing

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