RS369925361 COL11A1

Health Risk Chr 1:103025604
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Associated Conditions
Inborn genetic diseases
Marshall syndrome
Hearing loss
autosomal dominant 37
Fibrochondrogenesis
Stickler syndrome type 2
Inborn genetic diseases
Marshall syndrome
Hearing loss
autosomal dominant 37
Fibrochondrogenesis
Stickler syndrome type 2
Other Variants in COL11A1
rs121912943 rs121912944 rs2101038943 rs730882190 rs387906611 rs1557812993 rs398122828 rs56230601 rs398123652 rs587782990
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