ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.1194-16C>T

gnomAD frequency: 0.00004  dbSNP: rs754344039
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002116867 SCV002381672 likely benign RASopathy 2022-07-19 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003120816 SCV003800444 likely benign not provided 2022-03-21 criteria provided, single submitter clinical testing

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