RS202079239 CHRNB2

Health Risk Chr 1:154575801
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy
Inborn genetic diseases
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Lung function (FEV1) G OR: 5.07 4E-7 PubMed
Other Variants in CHRNB2
rs74315291 rs281865070 rs144813907 rs55685423 rs141735618 rs199885651 rs796052329 rs780175030 rs753731408 rs770055798
Ask Dr. Hemsworth about this variant