ClinVar Miner

Submissions for variant NM_001062.4(TCN1):c.401-9C>T

gnomAD frequency: 0.00579  dbSNP: rs66980105
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000956947 SCV001103739 benign Transcobalamin I deficiency 2024-01-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718793 SCV005324361 benign not provided criteria provided, single submitter not provided

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