RS797044949 COL1A2

Health Risk Chr 7:94412078
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in COL1A2
rs72656357 rs72659319 rs72659345 rs74315146 rs121912900 rs121912901 rs121912902 rs121912903 rs121912904 rs121912905
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