RS786205521 CRX

Health Risk Chr 19:47839341
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal dominant retinitis pigmentosa
Leber congenital amaurosis 7
Cone-rod dystrophy 2
Autosomal dominant retinitis pigmentosa
Leber congenital amaurosis 7
Cone-rod dystrophy 2
Other Variants in CRX
rs104894671 rs1568626209 rs104894672 rs61748436 rs104894673 rs2123743692 rs61748449 rs281865198 rs61748437 rs62636512
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