RS781936550 RP2

Health Risk Chr X:46853671
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Associated Conditions
Retinal dystrophy
Inborn genetic diseases
Retinal dystrophy
Inborn genetic diseases
Other Variants in RP2
rs137852284 rs104894925 rs28933687 rs104894926 rs2147081376 rs104894927 rs398124239 rs797044507 rs797044561 rs878853381
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