Table 1.
SNP | Position | pHW | MAF | Alleles (major/minor) | Feature |
---|---|---|---|---|---|
rs28947205 | 112,978,286 | 1.0 | 0.021 | C/T | intron |
rs12328178 | 112,978,391 | 1.0 | 0.013 | A/G | intron |
rs28947206 | 112,978,719 | 1.0 | 0.002 | G/T | intron |
rs28947207 | 112,978,748 | 1.0 | 0.011 | C/T | intron |
rs17042686 | 112,979,417 | 0.6071 | 0.066 | G/C | intron |
rs6707930 | 112,980,053 | 1.0 | 0.012 | C/A | missense (Gln34Lys) |
rs13410389 | 112,980,446 | 0.7871 | 0.085 | G/A | intron |
rs34216066 | 112,981,873 | 0.1303 | 0.095 | T/C | intron |
rs28947211 | 112,981,986 | 1.0 | 0.041 | T/C | intron |
rs13392494 | 112,982,098 | 0.175 | 0.464 | C/T | intron |
rs7584409 | 112,985,157 | 0.8851 | 0.31 | A/G | 3’ UTR |
pHW – Hardy-Weinberg p value
MAF – minor allele frequency among healthy controls
3’ UTR – 3′ untranslated region