ClinVar Miner

List of variants reported as pathogenic for Spinocerebellar ataxia type 21 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_001114748.2(TMEM240):c.509C>T (p.Pro170Leu)	rs606231451

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