Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 27 | ||
rs1009080 | 1 | 29958713 | intergenic variant | G/A | snv | 0.54 | 2 | ||||
rs10275045 | 0.882 | 0.160 | 7 | 1881190 | intron variant | C/T | snv | 0.35 | 5 | ||
rs10496702 | 2 | 133247997 | intron variant | G/A | snv | 0.18 | 2 | ||||
rs10949808 | 7 | 156255955 | intergenic variant | T/G | snv | 0.45 | 2 | ||||
rs11164835 | 1 | 92913536 | intron variant | G/A | snv | 0.35 | 2 | ||||
rs11740562 | 5 | 157515277 | intron variant | A/G | snv | 7.1E-02 | 2 | ||||
rs11789399 | 0.882 | 0.040 | 9 | 118597008 | intergenic variant | G/A;C | snv | 5 | |||
rs11789407 | 9 | 118597268 | intergenic variant | C/A | snv | 0.44 | 2 | ||||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs12201676 | 0.925 | 0.040 | 6 | 89022382 | regulatory region variant | T/C | snv | 0.21 | 4 | ||
rs12282742 | 11 | 18244252 | intron variant | C/G;T | snv | 2 | |||||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs12527359 | 6 | 89018502 | intergenic variant | T/A | snv | 0.23 | 2 | ||||
rs12745968 | 1 | 92936280 | intron variant | A/G | snv | 0.36 | 2 | ||||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
rs165599 | 0.677 | 0.280 | 22 | 19969258 | 3 prime UTR variant | G/A | snv | 0.56 | 27 | ||
rs165940 | 0.925 | 0.040 | 5 | 59383658 | intron variant | A/T | snv | 0.38 | 4 | ||
rs17069122 | 6 | 108002555 | downstream gene variant | G/A | snv | 1.9E-02 | 2 | ||||
rs17075286 | 3 | 43189231 | intergenic variant | C/G | snv | 5.9E-02 | 2 | ||||
rs17645023 | 1.000 | 0.040 | 17 | 66920916 | intergenic variant | A/T | snv | 0.22 | 3 | ||
rs17693963 | 0.882 | 0.040 | 6 | 27742386 | upstream gene variant | A/C;G | snv | 5 | |||
rs17746001 | 0.925 | 0.040 | 4 | 179734472 | intergenic variant | C/T | snv | 5.3E-02 | 4 | ||
rs1800497 | 0.620 | 0.400 | 11 | 113400106 | missense variant | G/A | snv | 0.26 | 0.26 | 56 | |
rs1801028 | 0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 | 24 |