Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
rs12075 | 0.724 | 0.240 | 1 | 159205564 | missense variant | G/A | snv | 0.51 | 0.66 | 3 | |
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 3 | |
rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 3 | ||
rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 2 | ||
rs11249433 | 0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv | 2 | |||
rs12405132 | 0.882 | 0.200 | 1 | 145790097 | intron variant | G/A | snv | 0.29 | 2 | ||
rs2235544 | 0.742 | 0.240 | 1 | 53909897 | intron variant | C/A;T | snv | 0.53; 4.0E-06 | 2 | ||
rs4245739 | 0.708 | 0.360 | 1 | 204549714 | 3 prime UTR variant | C/A;G | snv | 0.77; 6.2E-06 | 2 | ||
rs4971059 | 0.851 | 0.200 | 1 | 155176305 | intron variant | G/A | snv | 0.34 | 2 | ||
rs11205303 | 0.882 | 0.120 | 1 | 149934520 | missense variant | T/C | snv | 0.33 | 0.29 | 1 | |
rs11552449 | 0.925 | 0.080 | 1 | 113905767 | missense variant | C/G;T | snv | 0.22 | 0.15 | 1 | |
rs1205 | 0.602 | 0.680 | 1 | 159712443 | 3 prime UTR variant | C/T | snv | 0.30 | 1 | ||
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 1 | ||
rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 1 | |
rs2290854 | 0.925 | 0.080 | 1 | 204546897 | intron variant | A/G | snv | 0.65 | 0.57 | 1 | |
rs2494251 | 0.925 | 0.080 | 1 | 159311361 | downstream gene variant | G/A;C | snv | 1 | |||
rs616488 | 0.925 | 0.080 | 1 | 10506158 | intron variant | A/G | snv | 0.27 | 1 | ||
rs6678914 | 0.882 | 0.080 | 1 | 202218048 | intron variant | G/A | snv | 0.37 | 1 | ||
rs6682208 | 1.000 | 0.080 | 1 | 204597055 | intergenic variant | T/C | snv | 0.56 | 1 | ||
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 1 | |
rs844648 | 0.807 | 0.280 | 1 | 173254724 | regulatory region variant | G/A | snv | 0.46 | 1 | ||
rs903263 | 1.000 | 0.080 | 1 | 84156830 | intron variant | G/A;T | snv | 1 | |||
rs693 | 0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 | 7 | |
rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 6 |