RS1064797115 COL11A1

Health Risk Chr 1:103031245
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Hearing loss
autosomal dominant 37
Hearing impairment
Hearing loss
autosomal dominant 37
Hearing impairment
Other Variants in COL11A1
rs121912943 rs121912944 rs2101038943 rs730882190 rs387906611 rs1557812993 rs398122828 rs56230601 rs398123652 rs587782990
Ask Dr. Hemsworth about this variant