RS115913736 RELN
Upload your DNA to see your genotype for this variant.
Associated Conditions
Norman-Roberts syndrome
Familial temporal lobe epilepsy 7
RELN-related disorder
Norman-Roberts syndrome
Familial temporal lobe epilepsy 7
RELN-related disorder
Population Frequencies
gnomAD ALL
99.3%
1kG AFR
0.1%
1kG ALL
0.3%
1kG AMR
100%
1kG EAS
100%
1kG EUR
99.1%
1kG SAS
99.3%
Other Variants in RELN