Analysis of COCH and TNFA Variants in East Indian Primary Open-Angle Glaucoma Patients

Table 2

Variants identified in TNFA.

SNP ID	Location	Minor allele frequency (db SNP*)	Minor allele frequency in patients
rs4645838 ins C	5′ UTR	NA	0.02
rs3093662 A/G	Intron 1	0.079	0.01
rs3093664 A/G	Intron 3	0.075	0.005
rs4645845 C/T	3′ UTR	0.001	0.02

∗http://www.ncbi.nlm.nih.gov/projects/SNP/.