RS797044933 SCN3A

Health Risk Chr 2:165154514
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SCN3A
rs748935500 rs575814709 rs199975643 rs144957412 rs138766015 rs200538599 rs145171998 rs199597878 rs746501220 rs370141420
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