ClinVar Miner

Submissions for variant NM_015915.5(ATL1):c.1552-24_1552-20del

dbSNP: rs202061961
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001695053 SCV001906961 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260341 SCV002539619 benign Neuropathy, hereditary sensory, type 1D 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260340 SCV002539620 benign Hereditary spastic paraplegia 3A 2021-12-05 criteria provided, single submitter clinical testing

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