rs7823498

Parent Gene: NRG1

Importance: 3
Less common allele: C = 24%
More common allele: T = 76%
My Genotype: Log In
Risk Allele: T, T, T

Disease/Trait: Emphysema Imaging Measurement

The T allele of rs7823498 is reported to be associated with Emphysema Imaging Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Emphysema imaging phenotypes (Perc15, All).

Disease/Trait: Emphysema Imaging Measurement

The T allele of rs7823498 is reported to be associated with Emphysema Imaging Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Emphysema imaging phenotypes (%LAA-950, All).

Disease/Trait: Fev/Fec Ratio

The T allele of rs7823498 is reported to be associated with Fev/fec Ratio (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Post bronchodilator FEV1/FVC ratio in COPD.

Disease/Trait: Chronic Obstructive Pulmonary Disease

The T allele of rs7823498 is reported to be associated with Chronic Obstructive Pulmonary Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Post bronchodilator FEV1/FVC ratio in COPD.

Disease/Trait: Response To Bronchodilator

The T allele of rs7823498 is reported to be associated with Response To Bronchodilator (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Post bronchodilator FEV1/FVC ratio in COPD.