ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.353-2dup

dbSNP: rs1181503590
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000631232 SCV000752246 likely benign Cowden syndrome 2017-11-19 criteria provided, single submitter clinical testing

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