RS1903003 FAM13A

Health Risk Chr 4:88965145 snv intron variant

Upload your DNA to see your genotype for this variant.

What This Variant Does

"Association of FAM13A polymorphisms with COPD and COPD-related phenotypes in Han Chinese"

Associated Conditions

Chronic obstructive pulmonary disease

GWAS Studies (4)

Trait	Risk Allele	OR / Beta	P-value	Study
Chronic obstructive pulmonary disease	T	OR: 1.08	5E-9	PubMed
Post bronchodilator FEV1/FVC ratio	T	β: 0.01	2E-8	PubMed
Chronic obstructive pulmonary disease	T	OR: 1.08	3E-7	PubMed
Post bronchodilator FEV1	T	β: 0.04	5E-6	PubMed

Population Frequencies

1kG AFR

63%

1kG ALL

60%

1kG AMR

53.3%

1kG EAS

42.9%

1kG EUR

44.6%

1kG SAS

27%

Other Variants in FAM13A