Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6545977 | 0.882 | 0.160 | 2 | 63074029 | regulatory region variant | G/A | snv | 0.50 | 3 | ||
rs10496040 | 1.000 | 0.120 | 2 | 55080510 | 5 prime UTR variant | C/A | snv | 9.1E-02 | 1 | ||
rs117465650 | 1.000 | 0.120 | 2 | 55050090 | missense variant | C/T | snv | 0.12 | 6.1E-02 | 1 | |
rs17046583 | 1.000 | 0.120 | 2 | 55001811 | intron variant | A/G | snv | 6.8E-02 | 1 | ||
rs232228 | 1.000 | 0.120 | 2 | 88859459 | intron variant | G/A | snv | 0.15 | 1 | ||
rs232230 | 1.000 | 0.120 | 2 | 88857435 | missense variant | C/G | snv | 0.14 | 0.17 | 1 | |
rs2588519 | 1.000 | 0.120 | 2 | 54977988 | intron variant | T/C | snv | 0.68 | 1 | ||
rs2920891 | 1.000 | 0.120 | 2 | 55080901 | intron variant | C/A;T | snv | 1 | |||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs2228001 | 0.570 | 0.480 | 3 | 14145949 | missense variant | G/T | snv | 0.63 | 0.65 | 60 | |
rs2228000 | 0.585 | 0.560 | 3 | 14158387 | missense variant | G/A | snv | 0.24 | 0.21 | 53 | |
rs2660753 | 0.790 | 0.240 | 3 | 87061524 | intergenic variant | T/C | snv | 0.76 | 9 | ||
rs3755557 | 0.807 | 0.280 | 3 | 120096110 | non coding transcript exon variant | T/A | snv | 0.14 | 6 | ||
rs2073495 | 0.851 | 0.200 | 3 | 46439467 | missense variant | C/A;G | snv | 4.9E-04; 0.33 | 4 | ||
rs3864004 | 0.882 | 0.200 | 3 | 41198686 | 5 prime UTR variant | G/A | snv | 0.40 | 4 | ||
rs6774494 | 0.882 | 0.160 | 3 | 169364845 | intron variant | G/A | snv | 0.42 | 4 | ||
rs710521 | 0.851 | 0.200 | 3 | 189928144 | intergenic variant | T/C | snv | 0.24 | 4 | ||
rs9110 | 0.851 | 0.200 | 3 | 46439310 | missense variant | A/C;G;T | snv | 0.39 | 0.40 | 4 | |
rs10934853 | 0.882 | 0.160 | 3 | 128319530 | intron variant | C/A | snv | 0.43 | 3 | ||
rs17181170 | 0.882 | 0.160 | 3 | 87124174 | intron variant | G/A | snv | 0.38 | 3 | ||
rs2269432 | 0.882 | 0.120 | 3 | 50296800 | missense variant | T/A;G | snv | 0.13 | 3 | ||
rs189897 | 1.000 | 0.120 | 3 | 37477054 | intron variant | T/A | snv | 0.13 | 2 | ||
rs200046052 | 1.000 | 0.120 | 3 | 49902693 | missense variant | C/G;T | snv | 1.8E-04; 3.6E-05 | 2 | ||
rs169111 | 1.000 | 0.120 | 3 | 37474042 | intron variant | C/T | snv | 0.84 | 1 | ||
rs169188 | 1.000 | 0.120 | 3 | 37465958 | intron variant | G/A | snv | 7.6E-02 | 1 |