ClinVar Miner

Submissions for variant NM_005901.6(SMAD2):c.784+7T>A

gnomAD frequency: 0.00003  dbSNP: rs1429670443
Minimum review status: Collection method:
Minimum conflict level:
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 RCV002114106 SCV002438338 likely benign not provided 2022-06-30 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003331311 SCV004038971 uncertain significance not specified 2023-08-10 criteria provided, single submitter clinical testing

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