ClinVar Miner

Submissions for variant NM_001127511.3(APC):c.-55C>T

gnomAD frequency: 0.00001  dbSNP: rs1189950358
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003537043 SCV000647319 likely benign Familial adenomatous polyposis 1 2024-01-25 criteria provided, single submitter clinical testing

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