List of variants in gene SPTBN2 reported as uncertain significance for Autosomal recessive cerebellar ataxia

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 4

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HGVS	dbSNP
NM_006946.3(SPTBN2):c.2162G>A (p.Arg721His)	rs200016211
NM_006946.3(SPTBN2):c.3430C>T (p.Arg1144Ter)	rs1402216317
NM_006946.3(SPTBN2):c.3431G>A (p.Arg1144Gln)	rs558572111
NM_006946.3(SPTBN2):c.968A>G (p.Gln323Arg)	rs190532690

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