RS763295314 IMPG2

Health Risk Chr 3:101291499
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What This Variant Does
"CLNSIG=4
Associated Conditions
Vitelliform macular dystrophy 5
Autosomal recessive retinitis pigmentosa
Vitelliform macular dystrophy 5
Autosomal recessive retinitis pigmentosa
Other Variants in IMPG2
rs267606874 rs267606876 rs267606875 rs201893545 rs142710242 rs116450347 rs199867882 rs713993049 rs111784356 rs786205564
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