Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs524772 | 3 | 150729892 | downstream gene variant | G/A | snv | 0.98 | 2 | ||||
rs3108962 | 11 | 129895558 | 5 prime UTR variant | A/G | snv | 0.98 | 2 | ||||
rs34651 | 1.000 | 0.040 | 5 | 72848178 | non coding transcript exon variant | C/T | snv | 0.94 | 5 | ||
rs11133613 | 5 | 1074936 | intron variant | A/G | snv | 0.91 | 2 | ||||
rs7252007 | 19 | 10577081 | intron variant | T/C | snv | 0.90 | 2 | ||||
rs9438901 | 1 | 25258485 | intron variant | G/A | snv | 0.89 | 2 | ||||
rs1548770 | 14 | 74219855 | intergenic variant | C/T | snv | 0.88 | 2 | ||||
rs2370823 | 12 | 54138553 | intron variant | G/A | snv | 0.88 | 2 | ||||
rs2955088 | 3 | 128244867 | intron variant | C/T | snv | 0.86 | 4 | ||||
rs634454 | 9 | 108150874 | regulatory region variant | T/G | snv | 0.86 | 2 | ||||
rs2275707 | 1 | 219914705 | 3 prime UTR variant | C/A | snv | 0.85 | 2 | ||||
rs778986 | 1.000 | 0.080 | 19 | 5844526 | missense variant | A/G | snv | 0.84 | 0.84 | 3 | |
rs4951378 | 1 | 203689654 | intron variant | A/G | snv | 0.83 | 4 | ||||
rs6792151 | 3 | 171812145 | upstream gene variant | T/G | snv | 0.83 | 2 | ||||
rs1419114 | 1 | 203683316 | synonymous variant | A/G | snv | 0.88 | 0.83 | 3 | |||
rs10900586 | 1 | 203684957 | intron variant | G/A | snv | 0.83 | 2 | ||||
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
rs10883353 | 10 | 99496351 | intergenic variant | G/A | snv | 0.82 | 2 | ||||
rs380267 | 19 | 54295230 | upstream gene variant | G/A | snv | 0.82 | 3 | ||||
rs35995659 | 14 | 58287055 | intron variant | -/TT | ins | 0.82 | 2 | ||||
rs4703877 | 5 | 72430085 | intergenic variant | G/A | snv | 0.81 | 2 | ||||
rs2016409 | 5 | 151746763 | intron variant | G/T | snv | 0.81 | 2 | ||||
rs1029555 | 7 | 26547477 | upstream gene variant | T/C | snv | 0.80 | 2 | ||||
rs12449852 | 1.000 | 0.080 | 17 | 39475835 | intron variant | A/G | snv | 0.79 | 3 | ||
rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 15 |