ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.859-10A>T

gnomAD frequency: 0.00001  dbSNP: rs761341096
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000652826 SCV000774698 likely benign Noonan syndrome 9 2024-01-22 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003403502 SCV004121900 benign not specified 2023-10-19 criteria provided, single submitter clinical testing

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