Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs145905715 | 11 | 8100687 | intron variant | -/AT | delins | 3.5E-04 | 1 | ||||
rs3832016 | 1 | 109275536 | 3 prime UTR variant | -/T | ins | 0.74 | 3 | ||||
rs7203984 | 16 | 56965346 | intron variant | A/C | snv | 0.31 | 6 | ||||
rs16991720 | 21 | 34484464 | intron variant | A/C | snv | 4 | |||||
rs3858076 | 9 | 104893841 | intron variant | A/C | snv | 0.20 | 3 | ||||
rs585967 | 1.000 | 0.040 | 2 | 21047682 | upstream gene variant | A/C | snv | 0.81 | 3 | ||
rs34515106 | 2 | 68380846 | missense variant | A/C | snv | 6.7E-03 | 1.9E-03 | 2 | |||
rs11597086 | 10 | 100193948 | non coding transcript exon variant | A/C | snv | 0.30 | 0.29 | 1 | |||
rs17030613 | 1 | 112648185 | intron variant | A/C | snv | 0.19 | 1 | ||||
rs2737229 | 8 | 115636338 | intron variant | A/C | snv | 0.48 | 1 | ||||
rs4665710 | 2 | 20998163 | downstream gene variant | A/C | snv | 0.76 | 1 | ||||
rs556766 | 9 | 35089051 | 3 prime UTR variant | A/C | snv | 1.00 | 0.98 | 1 | |||
rs6987225 | 8 | 97963444 | intron variant | A/C | snv | 8.7E-02 | 1 | ||||
rs7849420 | 9 | 21499625 | intron variant | A/C | snv | 0.65 | 1 | ||||
rs8026235 | 15 | 88806225 | intron variant | A/C | snv | 1.7E-02 | 1 | ||||
rs9332492 | 1 | 169583872 | intron variant | A/C | snv | 4.8E-02 | 1 | ||||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
rs12113155 | 7 | 151607887 | intron variant | A/C;G | snv | 3 | |||||
rs13465 | 19 | 10692116 | 3 prime UTR variant | A/C;G | snv | 3 | |||||
rs598962 | 1 | 94451093 | intron variant | A/C;G | snv | 3 | |||||
rs655246 | 1 | 109289661 | downstream gene variant | A/C;G | snv | 3 | |||||
rs7162932 | 15 | 63060452 | intron variant | A/C;G | snv | 3 | |||||
rs11207995 | 1 | 62583880 | intron variant | A/C;G | snv | 2 | |||||
rs1168046 | 1 | 62518022 | intron variant | A/C;G | snv | 2 | |||||
rs1801689 | 17 | 66214462 | missense variant | A/C;G | snv | 4.0E-06; 2.4E-02; 4.8E-05 | 2 |