ClinVar Miner

Submissions for variant NM_001174150.2(ARL13B):c.486+22dup

dbSNP: rs368491848
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000860065 SCV000999986 benign not provided 2017-10-13 criteria provided, single submitter clinical testing
Mendelics RCV000987296 SCV001136558 benign Joubert syndrome 1 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV000860065 SCV001763776 likely benign not provided 2020-08-20 criteria provided, single submitter clinical testing

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