RS747050726 KCNQ2

Health Risk Chr 20:63442510
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in KCNQ2
rs28939683 rs74315390 rs28939684 rs74315391 rs267607198 rs74315392 rs118192244 rs118192200 rs118192217 rs118192218
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