ClinVar Miner

Submissions for variant NM_001034850.3(RETREG1):c.*455dup

dbSNP: rs140982908
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000386546 SCV000456155 benign Hereditary sensory and autonomic neuropathy type 2 2016-06-14 criteria provided, single submitter clinical testing

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