ClinVar Miner

Submissions for variant NM_003073.5(SMARCB1):c.362+8G>A

gnomAD frequency: 0.00001  dbSNP: rs727504162
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000153973 SCV000203598 uncertain significance not provided 2014-03-12 criteria provided, single submitter clinical testing
Invitae RCV000153973 SCV001098081 likely benign not provided 2023-09-05 criteria provided, single submitter clinical testing

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