Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10033900
rs10033900
CFI
0.010 GeneticVariation BEFREE One SNP (rs10033900) in the CFI gene, which encodes a protein involved in the inflammatory pathway, was significantly associated with myopic CNV in multivariate analysis after correction for multiple testing. 22678500

2012
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: 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: rs10453441
rs10453441
WNT7B
0.020 GeneticVariation BEFREE We identify WNT7B as a novel susceptibility gene for axial length (rs10453441, Pmeta=3.9 × 10(-13)) and corneal curvature (Pmeta=2.9 × 10(-40)) and confirm the previously reported association between GJD2 and myopia. 25823570

2015
dbSNP: rs10453441
rs10453441
WNT7B
0.020 GeneticVariation BEFREE WNT7B SNPs located in the same genomic region that includes rs9330813 have previously been associated with CCT in Latinos but with other ocular quantitative traits related to myopia (corneal curvature and axial length) in a Japanese population (rs10453441 and rs200329677). 29847655

2018
dbSNP: rs10462070
rs10462070
FGF10
0.010 GeneticVariation BEFREE Three FGF10 SNPs in complete linkage disequilibrium--rs339501, rs12517396, and rs10462070--were associated with extreme myopia in the Japanese population, and the risk allele of rs339501 differed from the previous Chinese population. 24265547

2013
dbSNP: rs10488
rs10488
MMP1 ; WTAPP1
0.010 GeneticVariation BEFREE Initial findings indicated that the best p values for each trait were 0.02 for myopia at rs2274755 (MMP9), 0.02 for SE at both rs3740938 (MMP8) and rs131451 (MMP11), 0.01 for axial length at rs11225395 (MMP8), 0.01 for anterior chamber depth at rs498186 (MMP1) and 0.02 at rs10488 (MMP1). 23077567

2012
dbSNP: rs104894910
rs104894910
NYX
0.010 GeneticVariation BEFREE The c.281G>C mutation cosegregated with nyctalopia and myopia. 16670814

2006
dbSNP: rs10500355
rs10500355
RBFOX1
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10511652
rs10511652
ADAMTSL1 ; LOC107986990
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10512441
rs10512441 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs1057518799
rs1057518799
POGZ
TGATTGGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518812
rs1057518812
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518829
rs1057518829
CACNA1F
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518848
rs1057518848
TCF4
CATTG 0.700 CausalMutation CLINVAR

dbSNP: rs1057518881
rs1057518881
FBN1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518891
rs1057518891
CHD7
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518909
rs1057518909
FBN1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518938
rs1057518938
MYH11 ; NDE1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1064583
rs1064583
COL10A1 ; NT5DC1
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs1064795104
rs1064795104
EXOC6B
C 0.700 GeneticVariation CLINVAR Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation. 23422942

2013
dbSNP: rs1064795104
rs1064795104
EXOC6B
C 0.700 GeneticVariation CLINVAR Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability. 25256811

2014
dbSNP: rs10824518
rs10824518
KCNMA1
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016