ClinVar Miner

Submissions for variant NM_173630.4(RTTN):c.4748-7A>G

gnomAD frequency: 0.00063  dbSNP: rs141673274
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
GeneDx RCV000879493 SCV000535579 likely benign not provided 2020-09-22 criteria provided, single submitter clinical testing
Invitae RCV000879493 SCV001022529 benign not provided 2024-01-17 criteria provided, single submitter clinical testing

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