{{Rsnum
|rsid=2736911
|Gene=ARMS2
|Chromosome=10
|position=124214355
|Orientation=plus
|GMAF=0.1295
|Gene_s=ARMS2
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 65.5 | 27.4 | 7.1
| HCB | 75.2 | 24.1 | 0.7
| JPT | 61.1 | 33.6 | 5.3
| YRI | 91.1 | 8.9 | 0.0
| ASW | 89.5 | 8.8 | 1.8
| CHB | 75.2 | 24.1 | 0.7
| CHD | 63.3 | 35.8 | 0.9
| GIH | 87.1 | 12.9 | 0.0
| LWK | 86.4 | 13.6 | 0.0
| MEX | 77.6 | 20.7 | 1.7
| MKK | 77.6 | 20.5 | 1.9
| TSI | 73.5 | 24.5 | 2.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=24013816
|Title=Cumulative association between age-related macular degeneration and less studied genetic variants in PLEKHA1/ARMS2/HTRA1: a meta and gene-cluster analysis
}}

{{PMID Auto
|PMID=16080115
|Title=Susceptibility genes for age-related maculopathy on chromosome 10q26.
|OA=1
}}

{{PMID Auto
|PMID=16642439
|Title=Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration.
|OA=1
}}

{{PMID Auto
|PMID=17903299
|Title=A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.
|OA=1
}}

{{PMID Auto
|PMID=18162041
|Title=Neovascular age-related macular degeneration risk based on CFH, LOC387715/HTRA1, and smoking.
|OA=1
}}

{{PMID Auto
|PMID=18688167
|Title=Polymorphisms in the LOC387715/ARMS2 putative gene and the risk for Alzheimer's disease.
}}

{{PMID Auto
|PMID=19259132
|Title=Multilocus analysis of age-related macular degeneration.
|OA=1
}}

{{PMID Auto
|PMID=19958499
|Title=A particle swarm based hybrid system for imbalanced medical data sampling.
|OA=1
}}

{{PMID Auto
|PMID=20140183
|Title=Genetic and functional dissection of HTRA1 and LOC387715 in age-related macular degeneration.
|OA=1
}}

{{PMID Auto
|PMID=20157352
|Title=Genetic analysis of typical wet-type age-related macular degeneration and polypoidal choroidal vasculopathy in Japanese population.
|OA=1
}}

{{PMID Auto
|PMID=20664794
|Title=Age-related macular degeneration-associated variants at chromosome 10q26 do not significantly alter ARMS2 and HTRA1 transcript levels in the human retina.
|OA=1
}}

{{PMID Auto
|PMID=21203342
|Title=Elevated C-reactive protein levels and ARMS2/HTRA1 gene variants in subjects without age-related macular degeneration.
|OA=1
}}

{{PMID Auto
|PMID=21252205
|Title=Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency.
|OA=1
}}

{{PMID Auto
|PMID=22293892
|Title=A69S and R38X ARMS2 and Y402H CFH gene polymorphisms as risk factors for neovascular age-related macular degeneration in Poland - a brief report.
|OA=1
}}

{{PMID Auto
|PMID=23289807
|Title=Gene-gene interactions of CFH and LOC387715/ARMS2 with Korean exudative age-related macular degeneration patients.
}}

{{PMID Auto
|PMID=25074467
|Title=Phenome-wide association studies (PheWASs) for functional variants
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}