ClinVar Miner

Submissions for variant NM_021008.4(DEAF1):c.294G>A (p.Val98=)

dbSNP: rs1038817783
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000501997 SCV000594349 uncertain significance not specified 2016-12-01 criteria provided, single submitter clinical testing
Invitae RCV002524176 SCV003018033 likely benign not provided 2023-06-29 criteria provided, single submitter clinical testing

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