ClinVar Miner

Submissions for variant NM_005633.4(SOS1):c.3195T>C (p.Tyr1065=)

dbSNP: rs1280224224
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005092847 SCV001082916 likely benign RASopathy 2024-02-20 criteria provided, single submitter clinical testing
GeneDx RCV000937140 SCV001874002 likely benign not provided 2021-02-26 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002222647 SCV002500702 likely benign not specified 2022-03-28 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002468095 SCV002763237 likely benign Noonan syndrome 4 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002468094 SCV002763238 likely benign Fibromatosis, gingival, 1 criteria provided, single submitter clinical testing

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