ClinVar Miner

Submissions for variant NM_005883.3(APC2):c.4260G>C (p.Gly1420=)

gnomAD frequency: 0.00283  dbSNP: rs148212035
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000949609 SCV001095870 benign not provided 2025-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000949609 SCV001985127 benign not provided 2021-10-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000949609 SCV005311290 benign not provided criteria provided, single submitter not provided

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