RS372989281 BEST1

Health Risk Chr 11:61958194
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Retinitis pigmentosa
Autosomal dominant vitreoretinochoroidopathy
Retinitis pigmentosa 50
Autosomal recessive bestrophinopathy
Vitelliform macular dystrophy 2
Retinal dystrophy
Retinitis pigmentosa
Autosomal dominant vitreoretinochoroidopathy
Retinitis pigmentosa 50
Autosomal recessive bestrophinopathy
Vitelliform macular dystrophy 2
Retinal dystrophy
Other Variants in BEST1
rs28940273 rs28940274 rs28941468 rs121918285 rs28941469 rs28940275 rs121918283 rs28940276 rs1805142 rs1800995
Ask Dr. Hemsworth about this variant