ClinVar Miner

Submissions for variant NM_002887.4(RARS1):c.1237-43dup

dbSNP: rs34318878
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
GeneDx RCV001534178 SCV001751081 benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796592 SCV002033448 benign Hypomyelinating leukodystrophy 9 2021-11-07 criteria provided, single submitter clinical testing

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