ClinVar Miner

Submissions for variant NM_020401.4(NUP107):c.1174+17del

dbSNP: rs200616275
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002093333 SCV002378976 benign not provided 2025-01-21 criteria provided, single submitter clinical testing
GeneDx RCV002093333 SCV004028144 likely benign not provided 2021-03-23 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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