ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.3568G>C (p.Val1190Leu) (rs876660708)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000222052 SCV000278349 uncertain significance Hereditary cancer-predisposing syndrome 2015-09-14 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence,In silico models in agreement (benign)

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