PPARG Polymorphisms Are Associated with Unexplained Mild Vision Loss in Patients with Type 2 Diabetes Mellitus

Table 1

Probe sequence for four SNPs used for Fluidigm sequencing analysis.

Rs number	SNP	Ch	Functional consequence	Position	SNP_SEQ
rs10865710	Intron C>G	3	Upstream transcript variant	12,311,699	AGTTTCATGTAGGTAAGACTGTGTAGAATGTCGGGTCTCGATGTTGGCGCTATTCAAGCCCTGATGATAAGGCTTTTGGCATTAGATGCTGTTTTGTCTT[C/G]ATGGAAAATACAGCTATTCTAGGATCCTTGAGCCTTTCATAAGAGATAAGGTTGTGAATCCTAAGACCCTAGGACCRTTTACTTAGATGATCTGCTCTCT
rs1801282	Intron C>G	3	Missense variant/coding sequence variant	12,351,626	TTGATCTTTTGCTAGATAGAGACAAAATATCAGTGTGAATTACAGCAAACCCCTATTCCATGCTGTTATGGGTGAAACTCTGGGAGATTCTCCTATTGAC[C/G]CAGAAAGCGATTCCTTCACTGATACACTGTCTGCAAACATATCACAAGGTAAAGTTCCTTCCAGATACGGCTATTGGGGACGTGGGGGCATTTATGTAAG
rs709158	Intron A>G	3	Genic downstream transcript variant	12,403,176	CTCTGCAGCAGGCAAAAGCTCTTTTTGTTAATTCAAAACAGTTTGGAATCCATTTCAGTTCTTCCTAAACCTCCAAGATACGGGGGAGGAAATTCACTGG[A/G]TTTTACAATATATTTTTCAAGGCAAATTGCCATCGCCGTCCTAATGACAGAGAAGCTGCCGATATCACTACAACGGCTGCAGATGGCAAGTCATCCAGCC
rs3856806	C1341T	3	3 prime UTR variant/synonymous variant	12,415,557	CCCTGGAGCTCCAGCTGAAGCTGAACCACCCTGAGTCCTCACAGCTGTTTGCCAAGCTGCTCCAGAAAATGACAGACCTCAGACAGATTGTCACGGAACA[C/T]GTGCAGCTACTGCAGGTGATCAAGAAGACGGAGACAGACATGAGTCTTCACCYGCTCCTGCAGGAGATCTACAAGGACTTGTACTAGCAGAGAGTCCTGA

Ch: chromosome.