ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.864+13A>G

gnomAD frequency: 0.00001  dbSNP: rs758808978
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002220148 SCV002363856 likely benign RASopathy 2023-09-19 criteria provided, single submitter clinical testing

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