ClinVar Miner

Submissions for variant NM_006922.4(SCN3A):c.2019+8T>C

gnomAD frequency: 0.00002  dbSNP: rs1159326316
Minimum review status: Collection method:
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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
CeGaT Center for Human Genetics Tuebingen RCV001311930 SCV001502313 uncertain significance not provided 2020-12-01 criteria provided, single submitter clinical testing
Invitae RCV001311930 SCV002391593 likely benign not provided 2023-08-31 criteria provided, single submitter clinical testing

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