RS201213623 TRPM1

Health Risk Chr 15:31060552
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Associated Conditions
Congenital stationary night blindness 1C
Inborn genetic diseases
TRPM1-related disorder
Congenital stationary night blindness 1C
Inborn genetic diseases
TRPM1-related disorder
Other Variants in TRPM1
rs766862238 rs267607140 rs267607141 rs191205969 rs387906862 rs786205113 rs772011426 rs138886378 rs376610188 rs727504182
Ask Dr. Hemsworth about this variant