ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.2057+34T>C

gnomAD frequency: 0.83210  dbSNP: rs3736761
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001725766 SCV001960785 benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810299 SCV002057535 benign Noonan syndrome 9 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001725766 SCV005289407 benign not provided criteria provided, single submitter not provided

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