RS749509661 CUL7

Health Risk Chr 6:43038323
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
3M syndrome 1
Inborn genetic diseases
3M syndrome 1
Other Variants in CUL7
rs121918228 rs121918229 rs730880261 rs730880301 rs730880262 rs730880263 rs201406974 rs786205581 rs200040003 rs786205651
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