RS759287748 COL11A1

Health Risk Chr 1:102887004
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Associated Conditions
Hearing loss
autosomal dominant 37
Inborn genetic diseases
Hearing loss
autosomal dominant 37
Inborn genetic diseases
Other Variants in COL11A1
rs121912943 rs121912944 rs2101038943 rs730882190 rs387906611 rs1557812993 rs398122828 rs56230601 rs398123652 rs587782990
Ask Dr. Hemsworth about this variant