Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893875 | 0.742 | 0.120 | 4 | 89828170 | missense variant | C/T | snv | 4.0E-06 | 13 | ||
rs201106962 | 0.851 | 0.080 | 4 | 89828156 | missense variant | A/C | snv | 8.0E-05 | 7.0E-05 | 5 | |
rs431905511 | 0.827 | 0.080 | 4 | 89828154 | missense variant | C/T | snv | 9 | |||
rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
rs542171324 | 0.851 | 0.160 | 4 | 89828148 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 6 | ||
rs2298728 | 1.000 | 0.040 | 4 | 89821664 | intron variant | G/A;T | snv | 1 | |||
rs894278 | 0.882 | 0.080 | 4 | 89813384 | intron variant | T/G | snv | 0.15 | 4 | ||
rs2197120 | 1.000 | 0.040 | 4 | 89808451 | intron variant | A/G | snv | 0.78 | 1 | ||
rs3775444 | 1.000 | 0.040 | 4 | 89805385 | intron variant | C/T | snv | 6.7E-02 | 1 | ||
rs3775442 | 1.000 | 0.040 | 4 | 89794080 | intron variant | C/T | snv | 6.7E-02 | 1 | ||
rs10014396 | 1.000 | 0.040 | 4 | 89791478 | intron variant | T/C | snv | 0.17 | 1 | ||
rs2737029 | 1.000 | 0.040 | 4 | 89790619 | intron variant | T/C | snv | 0.45 | 1 | ||
rs3775439 | 1.000 | 0.040 | 4 | 89788590 | intron variant | G/A | snv | 0.25 | 1 | ||
rs356186 | 1.000 | 0.040 | 4 | 89784213 | intron variant | A/G | snv | 0.80 | 1 | ||
rs356188 | 1.000 | 0.040 | 4 | 89770386 | intron variant | T/C | snv | 0.21 | 1 | ||
rs3796661 | 1.000 | 0.040 | 4 | 89766356 | intron variant | C/T | snv | 8.7E-02 | 1 | ||
rs10516845 | 1.000 | 0.040 | 4 | 89763127 | intron variant | A/G;T | snv | 1 | |||
rs2736990 | 0.882 | 0.080 | 4 | 89757390 | intron variant | G/A;T | snv | 4 | |||
rs3857059 | 1.000 | 0.040 | 4 | 89754087 | intron variant | A/G;T | snv | 2 | |||
rs356168 | 1.000 | 0.040 | 4 | 89753280 | intron variant | G/A | snv | 0.45 | 1 | ||
rs356200 | 0.882 | 0.160 | 4 | 89747463 | intron variant | T/C | snv | 0.44 | 4 | ||
rs356203 | 1.000 | 0.040 | 4 | 89744890 | intron variant | C/T | snv | 0.54 | 1 | ||
rs3822086 | 1.000 | 0.040 | 4 | 89743643 | intron variant | C/T | snv | 0.24 | 1 | ||
rs356204 | 1.000 | 0.040 | 4 | 89742391 | intron variant | T/C | snv | 0.44 | 1 | ||
rs3775423 | 1.000 | 0.040 | 4 | 89736340 | intron variant | C/T | snv | 0.24 | 1 |