ClinVar Miner

Submissions for variant NM_032730.5(RTN4IP1):c.1086C>T (p.Ile362=)

gnomAD frequency: 0.00019  dbSNP: rs200270996
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 RCV000945631 SCV001091667 benign not provided 2025-01-20 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000945631 SCV004159927 likely benign not provided 2023-05-01 criteria provided, single submitter clinical testing RTN4IP1: BP4, BP7

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