SNP ID | Chromosome | Functional Consequence | Nucleotide substitution | Primer sequences |
---|---|---|---|---|
rs7903146 | 10:112,998,590 | Intron variant | C > T | F: 5′- CAAATTCATGGGCTTTCT − 3′ R: 5′- CCTTCCCTGTAACTGTGG − 3′ |
rs11196205 | 10:113,047,288 | Intron variant | G > T | F: 5′- GAAAGT TCTCAACATTTATAACTTCG-3′ R: 5′- TTTGCCCAATAATATGCCATGAAA-3′ |
rs290487 | 10:113,149,972 | Intron variant | C > T | F: 5′- GCTGCCATATTGTTTACT − 3′ R: 5′- ATGATTTGTACTGGGTTG − 3′ |
rs12255372 | 10:113,049,143 | Intron variant | G > T | F: 5′- CTTGAGGTGTACTGGAAACTAAGGC-3′ R: 5′- CTGTCTATTTGGCATTCAAATGGA-3′ |