ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.2295-19G>C

gnomAD frequency: 0.00021  dbSNP: rs188003220
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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 RCV002093542 SCV002382429 likely benign Cowden syndrome 2024-10-23 criteria provided, single submitter clinical testing

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