Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11749040 | 0.827 | 0.120 | 5 | 40396323 | regulatory region variant | G/A | snv | 0.15 | 5 | ||
rs11749391 | 0.827 | 0.120 | 5 | 150849504 | intron variant | T/C | snv | 0.21 | 5 | ||
rs11750385 | 0.827 | 0.120 | 5 | 10521556 | intron variant | G/A;T | snv | 5 | |||
rs12075255 | 0.827 | 0.120 | 1 | 206788283 | intron variant | A/G | snv | 0.74 | 5 | ||
rs12131796 | 0.827 | 0.120 | 1 | 200909599 | intron variant | G/A | snv | 0.22 | 5 | ||
rs1250573 | 0.827 | 0.120 | 10 | 79282718 | intron variant | G/A | snv | 0.23 | 5 | ||
rs12694846 | 0.827 | 0.120 | 2 | 230283413 | intron variant | A/G | snv | 0.20 | 5 | ||
rs12879003 | 0.827 | 0.120 | 14 | 35359535 | downstream gene variant | T/A;G | snv | 0.43 | 5 | ||
rs1292035 | 0.827 | 0.120 | 17 | 59912196 | intron variant | G/A | snv | 0.16 | 5 | ||
rs12932970 | 0.827 | 0.120 | 16 | 85970504 | intron variant | T/C | snv | 0.29 | 5 | ||
rs12943464 | 0.827 | 0.120 | 17 | 47612985 | intron variant | A/T | snv | 0.45 | 5 | ||
rs12987977 | 0.827 | 0.120 | 2 | 102358876 | intron variant | T/G | snv | 0.31 | 5 | ||
rs13107612 | 0.827 | 0.120 | 4 | 101818823 | intron variant | C/T | snv | 0.31 | 5 | ||
rs1328454 | 0.827 | 0.120 | 20 | 49823486 | intron variant | T/C | snv | 0.57 | 5 | ||
rs140135 | 0.827 | 0.120 | 22 | 29767846 | non coding transcript exon variant | C/G | snv | 0.79 | 5 | ||
rs1405108 | 0.827 | 0.120 | 2 | 198880294 | downstream gene variant | C/A | snv | 0.61 | 5 | ||
rs141992399 | 0.827 | 0.120 | 9 | 136365140 | splice donor variant | C/G;T | snv | 3.3E-03; 4.0E-06 | 5 | ||
rs1525735 | 0.827 | 0.120 | 7 | 17157947 | intron variant | C/T | snv | 0.49 | 5 | ||
rs1551399 | 0.827 | 0.120 | 8 | 125527723 | intron variant | A/C | snv | 0.46 | 5 | ||
rs17229679 | 0.827 | 0.120 | 2 | 198696033 | intron variant | A/G | snv | 3.0E-02 | 5 | ||
rs17622517 | 0.827 | 0.120 | 5 | 132467845 | intron variant | T/C | snv | 5.4E-02 | 5 | ||
rs183686347 | 0.827 | 0.120 | 1 | 67237759 | intron variant | G/A | snv | 4.8E-03 | 5 | ||
rs196941 | 0.827 | 0.120 | 17 | 64069832 | non coding transcript exon variant | G/C;T | snv | 5 | |||
rs1992661 | 0.827 | 0.120 | 5 | 40414887 | upstream gene variant | G/A | snv | 0.58 | 5 | ||
rs201014116 | 0.827 | 0.120 | 2 | 25278036 | intron variant | C/A | snv | 6.6E-03 | 5 |