ClinVar Miner

Submissions for variant NM_000465.4(BARD1):c.159-14_159-13del

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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 RCV004018515 SCV004849346 uncertain significance Hereditary cancer-predisposing syndrome 2015-07-09 criteria provided, single submitter clinical testing The c.159-14_159-13delAT alteration is located in Intron 1 (E) of the BARD1 gene. This alteration consists of a deletion of 2 nucleotides at nucleotide position c.159-14 Intron 1 (E). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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