ClinVar Miner

List of variants reported as uncertain significance for Autosomal recessive spinocerebellar ataxia 10 by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_018075.5(ANO10):c.1133G>A (p.Arg378Gln)	rs61732728	0.00281
NM_018075.5(ANO10):c.88G>C (p.Glu30Gln)	rs147605535	0.00085
NM_018075.5(ANO10):c.1843G>A (p.Asp615Asn)	rs138000380	0.00035

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