ClinVar Miner

Submissions for variant NM_030928.4(CDT1):c.465C>T (p.Ala155=)

gnomAD frequency: 0.00397  dbSNP: rs202089169
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 RCV000970723 SCV001118316 benign not provided 2025-01-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000970723 SCV005252530 benign not provided criteria provided, single submitter not provided

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