RS886044555 COL2A1

Health Risk Chr 12:47985772
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Achondrogenesis type II
Inborn genetic diseases
Achondrogenesis type II
Other Variants in COL2A1
rs1555164872 rs121912864 rs121912865 rs121912866 rs121912867 rs2136528572 rs121912868 rs121912869 rs121912870 rs2136609285
Ask Dr. Hemsworth about this variant