RS398122828 COL11A1

Health Risk Chr 1:102915630
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What This Variant Does
"CLNSIG=5
Associated Conditions
Marshall syndrome
Inborn genetic diseases
COL11A1-related disorder
Stickler syndrome type 2
Marshall syndrome
Marshall syndrome
Inborn genetic diseases
COL11A1-related disorder
Stickler syndrome type 2
Marshall syndrome
Other Variants in COL11A1
rs121912943 rs121912944 rs2101038943 rs730882190 rs387906611 rs1557812993 rs56230601 rs398123652 rs587782990 rs147637674
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