{{Rsnum
|rsid=893817
|Gene=LOXL1
|Chromosome=15
|position=73936724
|Orientation=plus
|GMAF=0.3636
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=LOXL1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 39.8 | 40.7 | 19.5
| HCB | 24.8 | 50.4 | 24.8
| JPT | 25.7 | 51.3 | 23.0
| YRI | 54.4 | 36.7 | 8.8
| ASW | 50.9 | 33.3 | 15.8
| CHB | 24.8 | 50.4 | 24.8
| CHD | 22.9 | 44.0 | 33.0
| GIH | 49.5 | 41.6 | 8.9
| LWK | 42.7 | 47.3 | 10.0
| MEX | 46.6 | 37.9 | 15.5
| MKK | 50.6 | 39.1 | 10.3
| TSI | 46.1 | 48.0 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19584346
|Trait=Aortic root size
|Title=Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data
|RiskAllele=G
|Pval=0.000003
|OR=0.02
|ORtxt=[0.01-0.03] cm increase
|OA=1
}}

{{PMID|17690546}} Association between single nucleotide polymorphisms in the lysyl oxidase-like 1 gene and spontaneous cervical artery dissection.

{{PMID|18334928|OA=1
}} Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma.

{{PMID|18421074|OA=1
}} Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs893817
|overall_frequency_n=84
|overall_frequency_d=128
|overall_frequency=0.65625
|n_genomes=47
|n_genomes_annotated=0
|n_haplomes=68
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}