Table 1.
SNP | ChromosomeLocation | Gene | SNPFunction | GeneLocation | p-value | Minorallele | Majorallele | MAF |
---|---|---|---|---|---|---|---|---|
rs7447927 | 138861146 | TMEM173 | protein-coding | synonymous | 1.49E-36 | C | G | 34.7% |
rs13166214 | 138862744 | TMEM173 | protein-coding | 5’upstream | 8.92E-36 | A | G | 35.3% |
rs7444313 | 138865423 | TMEM173 | protein-coding | 5’upstream | 1.41E-35 | G | A | 34.5% |
rs13181561 | 138850905 | TMEM173 | protein-coding | 3’downstream | 1.81E-34 | G | A | 30.0% |
rs55792153 | 138854203 | TMEM173 | protein-coding | 3’downstream | 1.26E-32 | A | C | 34.2% |
rs13153461 | 138852369 | TMEM173 | protein-coding | 3’downstream | 2.61E-32 | G | A | 31.4% |
rs9716069 | 138842818 | ECSCR | protein-coding | 5’upstream | 5.32E-31 | T | A | 31.3% |
rs28419191 | 138844599 | ECSCR | protein-coding | 5’upstream | 1.50E-22 | T | C | 13.2% |
rs1131769 | 138857919 | TMEM173 | protein-coding | missense | 5.25E-22 | T | C | 14.0% |
rs11954057 | 138783832 | RNU5B-4P | pseudo | 3’downstream | 8.99E-22 | C | G | 32.5% |
rs36137978 | 138785565 | ECSCR | protein-coding | 5’upstream | 1.13E-21 | C | A | 31.6% |
rs10875554 | 138847652 | ECSCR | protein-coding | 5’upstream | 1.99E-21 | A | C | 15.4% |
rs6596479 | 138780599 | RNU5B-4P | pseudo | 5’upstream | 5.63E-21 | C | T | 31.9% |
rs7446197 | 138783734 | RNU5B-4P | pseudo | 3’downstream | 7.51E-21 | A | G | 33.8% |
rs10463977 | 138781765 | RNU5B-4P | pseudo | 5’upstream | 1.80E-20 | C | T | 32.4% |
rs2434576 | 138917674 | UBE2D2 | protein-coding | 5’upstream | 6.57E-17 | G | A | 30.8% |
rs34530489 | 138873627 | LOC642262 | pseudo | gene | 7.00E-17 | G | A | 31.4% |
rs35779874 | 138869847 | LOC642262 | pseudo | 5’upstream | 1.11E-16 | A | G | 31.2% |
rs7378724 | 138876953 | LOC642262 | pseudo | gene | 1.13E-16 | G | A | 30.9% |
rs78233829 | 138857925 | TMEM173 | protein-coding | missense | 3.16E-13 | G | C | 17.6% |
rs11554776 | 138861078 | TMEM173 | protein-coding | missense | 1.05E-12 | T | C | 16.5% |
rs7380824 | 138856982 | TMEM173 | protein-coding | missense | 1.25E-12 | T | C | 17.7% |
MAF, minor allele frequency. Bold, italics – SNP studied in this report. Bold – SNPs in HAQ STING haplotype.