RS1057518011 TMEM240

Health Risk Chr 1:1535766
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Spinocerebellar ataxia type 21
Inborn genetic diseases
Spinocerebellar ataxia type 21
Other Variants in TMEM240
rs606231451 rs606231452 rs606231454 rs606231455 rs1045410944 rs763953379 rs2100695149 rs779413548 rs765598128 rs755714285
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