RS199749070 SRRM2

Health Risk Chr 16:2766548
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SRRM2
rs2150776793 rs2150776534 rs2150777933 rs2150777403 rs2150776824 rs1464581573 rs2150778065 rs2150778293 rs2150778741 rs764663923
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