RS878853326 RP1

Health Risk Chr 8:54626631
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What This Variant Does
"CLNSIG=4
Associated Conditions
Retinal dystrophy
Inborn genetic diseases
Retinal dystrophy
Inborn genetic diseases
Other Variants in RP1
rs104894082 rs869320726 rs869320727 rs104894083 rs869320728 rs200860068 rs398124220 rs147680018 rs201493928 rs118031911
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