RS201176444 LIG4

Health Risk Chr 13:108208685
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in LIG4
rs104894418 rs104894419 rs104894420 rs104894421 rs587776663 rs142957638 rs886037777 rs772226399 rs770128720 rs529756815
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