ClinVar Miner

Submissions for variant NM_001160372.4(TRAPPC9):c.2475G>A (p.Arg825=)

dbSNP: rs756688439
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
Illumina Laboratory Services, Illumina RCV000390346 SCV000472185 uncertain significance Intellectual Disability, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000929098 SCV001074722 likely benign not provided 2024-05-23 criteria provided, single submitter clinical testing

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