RS797044915 COL11A2

Health Risk Chr 6:33176015
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in COL11A2
rs750995470 rs121912945 rs864309477 rs121912946 rs121912947 rs121912948 rs121912949 rs121912950 rs121912951 rs121912952
Ask Dr. Hemsworth about this variant