ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.214-10A>G

gnomAD frequency: 0.00017  dbSNP: rs371447614
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001451934 SCV001655576 likely benign RASopathy 2022-11-04 criteria provided, single submitter clinical testing
GeneDx RCV000542219 SCV001886151 benign not provided 2020-10-30 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002282229 SCV002570796 benign not specified 2022-07-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002467895 SCV002763598 benign Noonan syndrome 4 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002467894 SCV002763599 benign Fibromatosis, gingival, 1 criteria provided, single submitter clinical testing

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