Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2789588 | 6 | 72433995 | intergenic variant | A/C | snv | 0.26 | 1 | ||||
rs10462023 | 2 | 238275940 | intron variant | G/A | snv | 0.31 | 0.27 | 1 | |||
rs4583255 | 16 | 29977620 | intron variant | A/G | snv | 0.36 | 1 | ||||
rs1655285 | 1 | 231563728 | intron variant | G/C | snv | 9.5E-02 | 1 | ||||
rs1009080 | 1 | 29958713 | intergenic variant | G/A | snv | 0.54 | 2 | ||||
rs10949808 | 7 | 156255955 | intergenic variant | T/G | snv | 0.45 | 2 | ||||
rs12527359 | 6 | 89018502 | intergenic variant | T/A | snv | 0.23 | 2 | ||||
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 | ||||
rs1806864 | 9 | 87416754 | regulatory region variant | G/C | snv | 7.4E-02 | 2 | ||||
rs2018368 | 11 | 10718819 | intergenic variant | C/G | snv | 0.59 | 2 | ||||
rs2155907 | 11 | 98223945 | intergenic variant | C/T | snv | 0.38 | 2 | ||||
rs2509843 | 11 | 98254676 | intergenic variant | A/C;G;T | snv | 2 | |||||
rs2841307 | 6 | 100308811 | intergenic variant | C/T | snv | 0.20 | 2 | ||||
rs4996815 | 13 | 105999312 | intron variant | G/T | snv | 0.61 | 2 | ||||
rs6589386 | 1.000 | 0.040 | 11 | 113573031 | intergenic variant | C/T | snv | 0.36 | 2 | ||
rs6627057 | X | 145059799 | downstream gene variant | T/G | snv | 0.16 | 2 | ||||
rs6913660 | 1.000 | 0.040 | 6 | 27123646 | upstream gene variant | C/A | snv | 0.14 | 2 | ||
rs6932590 | 1.000 | 0.040 | 6 | 27281152 | downstream gene variant | T/C | snv | 0.26 | 2 | ||
rs7727102 | 5 | 4720472 | intron variant | G/C | snv | 0.32 | 2 | ||||
rs7912580 | 1.000 | 0.040 | 10 | 62156213 | regulatory region variant | G/A | snv | 7.6E-02 | 2 | ||
rs11740562 | 5 | 157515277 | intron variant | A/G | snv | 7.1E-02 | 2 | ||||
rs6024905 | 20 | 38329435 | intron variant | G/A | snv | 0.47 | 2 | ||||
rs245914 | 1.000 | 0.040 | 7 | 29178543 | intron variant | G/A;T | snv | 2 | |||
rs6444931 | 3 | 170445686 | intron variant | G/A | snv | 0.85 | 2 |