ClinVar Miner

Submissions for variant NM_005883.3(APC2):c.2845G>A (p.Ala949Thr)

gnomAD frequency: 0.03727  dbSNP: rs61735597
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
GeneDx RCV001616458 SCV001840182 benign not provided 2019-10-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001616458 SCV003339910 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001616458 SCV005311245 benign not provided criteria provided, single submitter not provided

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