ClinVar Miner

Submissions for variant NM_173630.4(RTTN):c.1929+3G>A

gnomAD frequency: 0.00767  dbSNP: rs75464253
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000968753 SCV000528421 benign not provided 2018-10-04 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000432521 SCV000596864 benign not specified 2017-10-24 criteria provided, single submitter clinical testing
Invitae RCV000968753 SCV001116225 benign not provided 2024-01-22 criteria provided, single submitter clinical testing

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