RS398124177 RPS6KA3

Health Risk Chr X:20187971
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What This Variant Does
"CLNSIG=5
Associated Conditions
Coffin-Lowry syndrome
Inborn genetic diseases
Coffin-Lowry syndrome
Inborn genetic diseases
Other Variants in RPS6KA3
rs122454124 rs122454125 rs122454126 rs587776755 rs122454127 rs1603426295 rs122454128 rs28935171 rs122454129 rs122454130
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