RS3126141 RP2

Health Risk Chr X:46853803 snv missense variant
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Population Frequencies
gnomAD ALL
100%
Other Variants in RP2
rs137852284 rs104894925 rs28933687 rs104894926 rs2147081376 rs104894927 rs398124239 rs797044507 rs797044561 rs878853381
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