Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9472135 | 0.925 | 0.120 | 6 | 43842065 | intron variant | T/A;C;G | snv | 9 | |||
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 9 | ||
rs62435145 | 1.000 | 0.040 | 7 | 1246931 | regulatory region variant | G/T | snv | 0.51 | 8 | ||
rs17476364 | 10 | 69334748 | intron variant | T/C | snv | 6.4E-02 | 8 | ||||
rs760077 | 0.925 | 0.120 | 1 | 155208991 | missense variant | T/A | snv | 0.36 | 8 | ||
rs2075672 | 7 | 100642673 | intron variant | A/G | snv | 0.65 | 8 | ||||
rs198846 | 6 | 26107235 | downstream gene variant | A/G;T | snv | 7 | |||||
rs129128 | 6 | 26125114 | intron variant | C/T | snv | 0.91 | 7 | ||||
rs9376090 | 6 | 135090090 | intron variant | T/C | snv | 0.19 | 7 | ||||
rs2000999 | 1.000 | 0.080 | 16 | 72074194 | intron variant | G/A | snv | 0.16 | 7 | ||
rs7203560 | 1.000 | 0.080 | 16 | 134391 | intron variant | T/G | snv | 2.0E-02 | 7 | ||
rs8887 | 1.000 | 0.080 | 19 | 4502189 | 3 prime UTR variant | T/C;G | snv | 0.51; 1.8E-05 | 7 | ||
rs130624 | 22 | 37042611 | regulatory region variant | G/T | snv | 0.47 | 6 | ||||
rs144861591 | 6 | 26072764 | intergenic variant | C/T | snv | 3.8E-02 | 6 | ||||
rs1533988 | 7 | 1253374 | intergenic variant | A/T | snv | 0.59 | 6 | ||||
rs218237 | 4 | 54528005 | intergenic variant | C/T | snv | 0.18 | 6 | ||||
rs147233090 | 0.925 | 0.040 | 15 | 43735849 | intron variant | C/T | snv | 1.7E-02 | 6 | ||
rs228129 | 22 | 37032558 | upstream gene variant | A/G | snv | 0.48 | 6 | ||||
rs10480300 | 0.925 | 0.120 | 7 | 151708919 | intron variant | C/T | snv | 0.24 | 6 | ||
rs2413450 | 22 | 37074184 | intron variant | T/C | snv | 0.61 | 6 | ||||
rs198833 | 6 | 26114280 | downstream gene variant | G/A | snv | 0.87 | 5 | ||||
rs218264 | 4 | 54542708 | intergenic variant | A/G;T | snv | 5 | |||||
rs632057 | 6 | 139512875 | intron variant | T/G | snv | 0.57 | 5 | ||||
rs442177 | 4 | 87109109 | intron variant | G/T | snv | 0.56 | 5 | ||||
rs3218097 | 6 | 41937537 | intron variant | G/A;T | snv | 5 |