ClinVar Miner

List of variants studied for Spinocerebellar ataxia, autosomal recessive 21 by OMIM

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Total variants: 4
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HGVS dbSNP
NM_020680.4(SCYL1):c.1433A>G (p.Asp478Gly) rs1554969925
NM_020680.4(SCYL1):c.169C>T (p.Gln57Ter) rs1554967681
NM_020680.4(SCYL1):c.1882C>T (p.Gln628Ter) rs1554970375
NM_020680.4(SCYL1):c.314C>T (p.Ala105Val) rs942522644

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