RS786205229 SNX14

Health Risk Chr 6:85543737
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive spinocerebellar ataxia 20
Spinocerebellar atrophy
Autosomal recessive spinocerebellar ataxia 20
Spinocerebellar atrophy
Other Variants in SNX14
rs876657385 rs869320748 rs876657386 rs876657387 rs774694340 rs201128942 rs1057519561 rs749656742 rs1554226470 rs1064793681
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