ClinVar Miner

Submissions for variant KIF1A, 1-BP DUP, 5271C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000023086 SCV000044377 pathogenic Hereditary sensory and autonomic neuropathy type IIC 2011-08-12 no assertion criteria provided literature only

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