ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.721G>A (p.Glu241Lys)

gnomAD frequency: 0.00009  dbSNP: rs148747022
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
Invitae RCV000691771 SCV000819562 likely benign Noonan syndrome 9 2023-11-02 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000691771 SCV003822091 uncertain significance Noonan syndrome 9 2020-02-18 criteria provided, single submitter clinical testing

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