ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.3360C>A (p.Val1120=)

gnomAD frequency: 0.00002  dbSNP: rs751042920
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 RCV001422995 SCV001625561 likely benign RASopathy 2024-02-06 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005237802 SCV005884778 likely benign not specified 2024-12-06 criteria provided, single submitter clinical testing

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