RS116448158 CNGA3

Health Risk Chr 2:98396787 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Achromatopsia
Achromatopsia 2
CNGA3-related disorder
Retinal dystrophy
Achromatopsia
Achromatopsia 2
CNGA3-related disorder
Retinal dystrophy
Population Frequencies
gnomAD ALL
99.8%
1kG AFR
100%
1kG ALL
99.9%
1kG AMR
100%
1kG EAS
100%
1kG EUR
99.7%
1kG SAS
100%
Other Variants in CNGA3
rs104893612 rs104893613 rs104893614 rs104893615 rs104893616 rs104893617 rs137852608 rs104893619 rs104893620 rs104893621
Ask Dr. Hemsworth about this variant