RS184399988 COL11A2

Health Risk Chr 6:33167098
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Associated Conditions
Hearing impairment
Inborn genetic diseases
Hearing impairment
Inborn genetic diseases
Other Variants in COL11A2
rs750995470 rs121912945 rs864309477 rs121912946 rs121912947 rs121912948 rs121912949 rs121912950 rs121912951 rs121912952
Ask Dr. Hemsworth about this variant