ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.859-4del

dbSNP: rs776327707
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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 RCV001510718 SCV001717825 benign Noonan syndrome 9 2019-11-27 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003326583 SCV004033294 likely benign not provided 2023-07-01 criteria provided, single submitter clinical testing SOS2: BP4, BS1

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