ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.960A>G (p.Leu320=)

dbSNP: rs886038279
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
PreventionGenetics, part of Exact Sciences RCV000249309 SCV000303574 benign not specified criteria provided, single submitter clinical testing

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