RS267606794 FAM161A

Health Risk Chr 2:61840319
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Retinitis pigmentosa 28
Retinal dystrophy
Autosomal recessive retinitis pigmentosa
Retinitis pigmentosa 28
Retinal dystrophy
Autosomal recessive retinitis pigmentosa
Other Variants in FAM161A
rs200691042 rs397704718 rs202193201 rs267606793 rs139266382 rs187695569 rs77562614 rs145199539 rs761440783 rs369633003
Ask Dr. Hemsworth about this variant