RS3825942 LOXL1

Health Risk Chr 15:73927241
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What This Variant Does
"rs3825942, also known as G153D, a SNP causing an amino acid change in the lysyl oxidase 1 LOXL1 gene...
Associated Conditions
Exfoliation syndrome
susceptibility to
LOXL1-related disorder
Exfoliation syndrome
susceptibility to
LOXL1-related disorder
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
Glaucoma (primary open-angle) — OR: 0.15 5E-35 PubMed
Glaucoma (exfoliation) G OR: 20.1 3E-21 PubMed
Other Variants in LOXL1
rs1048661 rs2165241
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