RS780237166 CNGB1

Health Risk Chr 16:57960065
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Associated Conditions
Inborn genetic diseases
Retinal dystrophy
Inborn genetic diseases
Retinal dystrophy
Other Variants in CNGB1
rs121918532 rs1567360969 rs1052029 rs372504780 rs527236060 rs527236061 rs201162411 rs192628905 rs146170855 rs148735841
Ask Dr. Hemsworth about this variant