ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.353T>A (p.Leu118Ter)

dbSNP: rs1825725461
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV001263719 SCV001441812 likely pathogenic Fanconi anemia complementation group C 2019-10-24 criteria provided, single submitter clinical testing

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