ClinVar Miner

Submissions for variant NM_024675.3(PALB2):c.2473A>G (p.Arg825Gly) (rs745747228)

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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 RCV000454362 SCV000538153 uncertain significance Hereditary cancer-predisposing syndrome 2014-10-03 criteria provided, single submitter clinical testing Insufficient or conflicting evidence
Fulgent Genetics,Fulgent Genetics RCV000764048 SCV000895002 uncertain significance Familial cancer of breast; Fanconi anemia, complementation group N; Pancreatic cancer 3 2018-10-31 criteria provided, single submitter clinical testing

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