ClinVar Miner

Submissions for variant NM_021942.6(TRAPPC11):c.2851+42GC[2]

dbSNP: rs147708886
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001690181 SCV001910569 benign not provided 2019-05-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838789 SCV002098699 benign Autosomal recessive limb-girdle muscular dystrophy type R18 2021-09-10 criteria provided, single submitter clinical testing

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