ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.2162-16T>C

gnomAD frequency: 0.00004  dbSNP: rs764585497
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002154546 SCV002465723 likely benign Noonan syndrome 9 2024-10-07 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005058120 SCV005725521 likely benign not specified 2024-11-29 criteria provided, single submitter clinical testing

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