RS61754044 ABCA4

Health Risk Chr 1:94030992
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Retinal dystrophy
Severe early-childhood-onset retinal dystrophy
Stargardt disease
Retinitis pigmentosa 19
Inborn genetic diseases
Retinal dystrophy
Severe early-childhood-onset retinal dystrophy
Stargardt disease
Retinitis pigmentosa 19
Other Variants in ABCA4
rs58331765 rs61751408 rs61749438 rs61750061 rs61750064 rs1800553 rs61751386 rs28938473 rs61753034 rs61751374
Ask Dr. Hemsworth about this variant