RS886042856 COL6A1

Health Risk Chr 21:45989084
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in COL6A1
rs121912934 rs886042354 rs797044456 rs121912935 rs121912936 rs398123631 rs1569517717 rs797044457 rs797044458 rs121912937
Ask Dr. Hemsworth about this variant