RS797044917 OFD1

Health Risk Chr X:13749527
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in OFD1
rs122460150 rs312262822 rs312262833 rs312262886 rs312262890 rs312262895 rs312262894 rs398122866 rs312262863 rs312262809
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