ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.693T>C (p.Asp231=)

dbSNP: rs2139733831
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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 RCV002096555 SCV002394801 likely benign Noonan syndrome 9 2023-06-06 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003389899 SCV004134090 uncertain significance not provided 2022-09-01 criteria provided, single submitter clinical testing SOS2: PM2:Supporting, BP4

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