ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.1443C>T (p.Tyr481=)

gnomAD frequency: 0.00001  dbSNP: rs755043578
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002541554 SCV001073086 likely benign Noonan syndrome 9 2022-09-18 criteria provided, single submitter clinical testing

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