ClinVar Miner

Submissions for variant NM_000038.6(APC):c.8184G>A (p.Val2728=)

dbSNP: rs1766673977
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001182124 SCV001347478 likely benign Hereditary cancer-predisposing syndrome 2019-01-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV004564605 SCV001625692 likely benign Familial adenomatous polyposis 1 2024-07-06 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004564605 SCV005082977 benign Familial adenomatous polyposis 1 2024-04-12 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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