ClinVar Miner

Submissions for variant NM_001352754.2(ARMC9):c.2205dup (p.Thr736fs)

dbSNP: rs35889244
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 RCV001517860 SCV001726448 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001554106 SCV001775278 benign Joubert syndrome 30 2021-07-14 criteria provided, single submitter clinical testing

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