ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1744-14_1744-13del

dbSNP: rs1554083086
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000663147 SCV000786295 likely benign Familial adenomatous polyposis 1 2018-04-11 criteria provided, single submitter clinical testing

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