ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.1624G>C (p.Glu542Gln)

dbSNP: rs121913273
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
German Consortium for Hereditary Breast and Ovarian Cancer, University Hospital Cologne RCV000785596 SCV000924171 pathogenic Ovarian neoplasm 2018-12-01 no assertion criteria provided research

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