RS200684841 TRPM1

Health Risk Chr 15:31037797
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Associated Conditions
Inborn genetic diseases
Optic atrophy
Inborn genetic diseases
Optic atrophy
Other Variants in TRPM1
rs766862238 rs267607140 rs267607141 rs191205969 rs387906862 rs786205113 rs772011426 rs138886378 rs376610188 rs727504182
Ask Dr. Hemsworth about this variant