ClinVar Miner

Submissions for variant NM_013236.4(ATXN10):c.404G>T (p.Gly135Val)

gnomAD frequency: 0.00016  dbSNP: rs199766375
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
O&I group, Department of Genetics, University Medical Center of Groningen RCV001849214 SCV001960856 uncertain significance Spinocerebellar ataxia type 10 2021-07-22 no assertion criteria provided research

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