Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs524952
rs524952 		0.710 GeneticVariation BEFREE Moreover, 15q14 variant rs524952 (p=0.015, OR=1.49) also showed mild association with myopia and high myopia. 31604699

2019
dbSNP: rs524952
rs524952 		0.710 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10089517
rs10089517 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10113215
rs10113215 		0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. 25233373

2014
dbSNP: rs10512441
rs10512441 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs11658305
rs11658305 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs1370156
rs1370156 		0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. 25233373

2014
dbSNP: rs1556867
rs1556867 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs61049169
rs61049169 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs73157695
rs73157695 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs9585327
rs9585327 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10034228
rs10034228 		0.020 GeneticVariation BEFREE Genotype and allele frequencies of the four SNPs showed significant differences between the myopia and control groups (rs2218817: genotype p = 0.009, OR = 1.18; rs10034228: genotype p = 0.009, OR = 1.18; rs1585471: genotype p = 0.007, OR = 1.19 and rs6837348: genotype p = 0.012, OR = 1.18). 22150588

2012
dbSNP: rs10034228
rs10034228 		0.020 GeneticVariation BEFREE The 4q25 variant rs10034228 (p=0.002, OR=0.56) and <i>MIPEP</i> variant rs9318086 (p=0.004, OR=1.62) were found to be significantly associated with myopia as well as different severity of myopia. 31604699

2019
dbSNP: rs634990
rs634990 		0.020 GeneticVariation BEFREE Persons with combinations of genotypes rs634990 CC and rs8027411 GT have 2.7 times higher odds to have myopia. 29793445

2018
dbSNP: rs634990
rs634990 		0.020 GeneticVariation BEFREE The risk of myopia versus hyperopia was OR 1.88 (95 % CI 1.64, 2.16, P < 0.001) for homozygous carriers of the risk allele at the top SNP rs634990, and OR 1.33 (95 % CI 1.19, 1.49, P < 0.001) for heterozygous carriers. 22665138

2012
dbSNP: rs10936538
rs10936538 		0.010 GeneticVariation BEFREE Association was also significant for myopia (best association: OR = 0.80; 95% CI, 0.69-0.93; P = 0.003 for rs10936538). 22110064

2012
dbSNP: rs1585471
rs1585471 		0.010 GeneticVariation BEFREE Genotype and allele frequencies of the four SNPs showed significant differences between the myopia and control groups (rs2218817: genotype p = 0.009, OR = 1.18; rs10034228: genotype p = 0.009, OR = 1.18; rs1585471: genotype p = 0.007, OR = 1.19 and rs6837348: genotype p = 0.012, OR = 1.18). 22150588

2012
dbSNP: rs2218817
rs2218817 		0.010 GeneticVariation BEFREE Genotype and allele frequencies of the four SNPs showed significant differences between the myopia and control groups (rs2218817: genotype p = 0.009, OR = 1.18; rs10034228: genotype p = 0.009, OR = 1.18; rs1585471: genotype p = 0.007, OR = 1.19 and rs6837348: genotype p = 0.012, OR = 1.18). 22150588

2012
dbSNP: rs4373767
rs4373767 		0.010 GeneticVariation BEFREE The risk allele T of <i>ZC3H11B</i> SNP rs4373767 was significantly associated with high myopia (OR=1.39, p=0.007) and extreme myopia (OR=1.34, p=0.013) when compared with controls, whereas <i>ZFHX1B</i> rs13382811 (allele T, OR=1.33, p=0.018) and <i>SNTB1</i> rs7839488 (allele G, OR=1.71, p=8.44E-05) were significantly associated with extreme myopia only. 31300455

2019
dbSNP: rs6837348
rs6837348 		0.010 GeneticVariation BEFREE Genotype and allele frequencies of the four SNPs showed significant differences between the myopia and control groups (rs2218817: genotype p = 0.009, OR = 1.18; rs10034228: genotype p = 0.009, OR = 1.18; rs1585471: genotype p = 0.007, OR = 1.19 and rs6837348: genotype p = 0.012, OR = 1.18). 22150588

2012
dbSNP: rs10511652
rs10511652
ADAMTSL1 ; LOC107986990
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs864321670
rs864321670
ALDH18A1
T 0.700 CausalMutation CLINVAR

dbSNP: rs8027411
rs8027411
ANKRD34C-AS1
0.010 GeneticVariation BEFREE Persons with combinations of genotypes rs634990 CC and rs8027411 GT have 2.7 times higher odds to have myopia. 29793445

2018
dbSNP: rs7162310
rs7162310
APH1B
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs387907141
rs387907141
ARID1B
T 0.700 CausalMutation CLINVAR