ClinVar Miner

Submissions for variant NM_018075.5(ANO10):c.1915-5852T>C

gnomAD frequency: 0.97895  dbSNP: rs6441771
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001554158 SCV001775345 benign Autosomal recessive spinocerebellar ataxia 10 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001638164 SCV001852145 benign not provided 2019-09-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001638164 SCV005241102 benign not provided criteria provided, single submitter not provided

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