Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1550094
rs1550094
PRSS56
0.710 GeneticVariation BEFREE We also found evidence of association with spherical equivalent on 2q37.1 in PRSS56 at rs1550094 (MAF = 31%, β = -0.33, p = 1.7 × 10(-3)), a region previously associated with myopia. 27440996

2016
dbSNP: rs1550094
rs1550094
PRSS56
0.710 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
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: rs7744813
rs7744813
KCNQ5
0.710 GeneticVariation BEFREE The SNP rs7744813, previously shown to be associated with refractive error and myopia in two GWAS, showed an odds ratio of 0.75 (95% CI 0.63-0.90; <i>P</i><sub>emp</sub> = 0.0058) for the minor allele. 28884119

2017
dbSNP: rs7744813
rs7744813
KCNQ5
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: 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: rs1057518829
rs1057518829
CACNA1F
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518881
rs1057518881
FBN1
A 0.700 GeneticVariation 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
dbSNP: rs1085307138
rs1085307138
PUF60 ; SCRIB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs10887265
rs10887265
RGR
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10892173
rs10892173
FXYD2 ; DSCAML1 ; LOC107984394
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs11145488
rs11145488
TJP2
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs11606250
rs11606250
LRRC4C
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