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. Author manuscript; available in PMC: 2020 Jan 1.
Published in final edited form as: Ophthalmology. 2018 Oct 21;126(1):38–48. doi: 10.1016/j.ophtha.2018.10.031

Table 3.

Summary of Findings

Gene SNP in this report Phenotype Relationship(s) to previously reported SNPs for POAG
TGFBR3 rs11466588 POAG No LD with prior rs2810903.
TMCO1 rs10529326 POAG In LD with prior rs4656461 and prior rs7518099.9
MYOC rs12129856 POAG No association observed with previously published SNPs. SNP is located in adjacent gene, PRRC2C. (Fig. 4)
CYP1B1 rs2432663 POAG rs2432663 is located between CYP1B1 and CYP1B1-AS1.
FNDC3B rs199612704 POAG No LD with prior rs12897; separated by region of high recombination (Fig. 3A&B).
AFAP1 rs4328916 POAG No LD with prior rs4619890.24
8q22 rs7009228 POAG No LD with previously reported rs1521444, rs284489, or rs284495.14 Closer to LRP12 gene.
9p21 rs2383204,
rs79721419
POAG Two independent signals identified. Signal #1 at rs2383204 is in linkage disequilibrium with previously published SNPS rs1063192 42 and rs4977756.9 Signal #2 at rs79721419 is approximately 150kb away from #1 and separated by a region of high recombination (Fig. 2)
ENO4 rs185815146 Advanced
POAG
Putative novel locus for AD POAG
ABO rs551169 POAG No LD with prior rs8176743; located in ABO promoter.39
PMM2 rs13332985 Advanced
POAG
No LD with prior rs3785176 or rs8057024.11
GAS7 rs8080535 Advanced
POAG
No LD with prior rs12150284; separated by region of high recombination (Fig. 3C&D).54

Note: Linkage disequilibrium (LD) between SNPs was assessed using the “AMR” subset of the 1kGP data. This set will contain genomic segments from African, Amerindian, European ancestry. “Prior” indicates SNPs reported to be genome-wide significant in a genome-wide association study.