ClinVar Miner

Submissions for variant NM_014822.4(SEC24D):c.2959-15dup

dbSNP: rs140990828
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 RCV001689524 SCV001915222 benign not provided 2019-08-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807511 SCV002054727 benign Cole-Carpenter syndrome 2 2021-07-15 criteria provided, single submitter clinical testing
Invitae RCV001689524 SCV002348867 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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