RS869312965 GLI2

Health Risk Chr 2:120955349
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in GLI2
rs121917707 rs121917708 rs398122882 rs587777455 rs587777456 rs374155310 rs145778937 rs200831069 rs141988240 rs377700501
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