RS201849628 GNAT1

Health Risk Chr 3:50193356
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Associated Conditions
Congenital stationary night blindness autosomal dominant 3
Inborn genetic diseases
Congenital stationary night blindness autosomal dominant 3
Inborn genetic diseases
Other Variants in GNAT1
rs1460825110 rs143481438 rs2109138350 rs753761683 rs571471319 rs769750483 rs2109139201 rs534226069 rs190126440 rs1440003996
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