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TYR
位点：RS1042602
ARMS2
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RBFOX1
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TJP2
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PDE11A
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PTPN5
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KIRREL
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PRSS56
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ZBTB38
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COL10A1
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CASC15
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VIPR2
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BICC1
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DLG2
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GRIN2B
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CPSF2
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BMP3
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KAZALD1
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COL4A4
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SNTB1
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Insights into the genetic basis of retinal detachment
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Detection and interpretation of shared genetic influences on 42 human traits
Detection and interpretation of shared genetic influences on 42 human traits
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Insights into the genetic basis of retinal detachment
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Whole exome sequence analysis in 51624 participants identifies novel genes and variants associated with refractive error and myopia
Association of the ZC3H11B, ZFHX1B and SNTB1 genes with myopia of different severities
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