RS145522851 SPTBN2
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What This Variant Does
"aka R2370H Classified by ACMG guidelines as of 'uncertain significance' for a form of spinocerebella..."
Associated Conditions
Autosomal recessive spinocerebellar ataxia 14
Spinocerebellar ataxia type 5
Inborn genetic diseases
Autosomal recessive spinocerebellar ataxia 14
Spinocerebellar ataxia type 5
Inborn genetic diseases
Other Variants in SPTBN2