ClinVar Miner

Submissions for variant NM_007373.4(SHOC2):c.1423-15T>C

gnomAD frequency: 0.00004  dbSNP: rs775689426
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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 RCV002162581 SCV002419038 likely benign RASopathy 2023-10-04 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002509754 SCV002819438 uncertain significance not specified 2022-12-11 criteria provided, single submitter clinical testing

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