ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.659_660del (p.Ser220fs)

dbSNP: rs1575577384
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City RCV001028055 SCV001190828 uncertain significance Noonan syndrome 5 2020-02-05 no assertion criteria provided clinical testing

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