ClinVar Miner

Submissions for variant NM_000314.6(PTEN):c.-862G>T

dbSNP: rs587781706
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000129879 SCV000184696 uncertain significance Hereditary cancer-predisposing syndrome 2014-03-05 criteria provided, single submitter clinical testing
GeneDx RCV002051812 SCV002319137 uncertain significance not provided 2023-09-11 criteria provided, single submitter clinical testing Has not been previously published as pathogenic or benign to our knowledge; No data available from control populations to assess the frequency of this variant; Also known as c.-862G>T

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