Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10038095 | 5 | 75341886 | intron variant | A/T | snv | 0.38 | 3 | ||||
rs1006725 | 10 | 112970444 | intron variant | A/G | snv | 4.2E-03 | 2 | ||||
rs10087178 | 8 | 10111284 | intron variant | T/C | snv | 6.6E-02 | 2 | ||||
rs10102164 | 8 | 54509054 | upstream gene variant | G/A | snv | 0.19 | 3 | ||||
rs10107815 | 8 | 10156645 | intron variant | G/C | snv | 5.1E-02 | 4 | ||||
rs10156121 | 7 | 142672656 | downstream gene variant | T/C | snv | 3.9E-02 | 4 | ||||
rs10199768 | 2 | 21021128 | intron variant | G/T | snv | 0.35 | 5 | ||||
rs10212320 | 3 | 30632373 | non coding transcript exon variant | C/T | snv | 7.2E-03 | 2 | ||||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs10260606 | 7 | 44544952 | upstream gene variant | G/A;C | snv | 2 | |||||
rs10271556 | 7 | 106258428 | intron variant | C/T | snv | 5.6E-02 | 4 | ||||
rs10306121 | 9 | 122372369 | intron variant | A/T | snv | 6.5E-02 | 2 | ||||
rs10306137 | 9 | 122376185 | intron variant | C/T | snv | 1.8E-02 | 3 | ||||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 6 | ||
rs10402271 | 1.000 | 0.080 | 19 | 44825957 | downstream gene variant | T/G | snv | 0.28 | 6 | ||
rs10402729 | 19 | 19244291 | intron variant | T/C | snv | 3.3E-02 | 4 | ||||
rs10415849 | 19 | 19394278 | intron variant | C/T | snv | 0.12 | 4 | ||||
rs1041968 | 2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 | 4 | |||
rs1042031 | 0.790 | 0.200 | 2 | 21002881 | stop gained | C/A;T | snv | 8.0E-06; 0.15 | 3 | ||
rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 7 | |
rs10433493 | 3 | 190647811 | intron variant | G/C | snv | 1.8E-02 | 2 | ||||
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 6 | ||
rs10474434 | 5 | 75348856 | intron variant | G/T | snv | 0.20 | 3 | ||||
rs10478730 | 6 | 12297276 | downstream gene variant | C/T | snv | 1.2E-02 | 5 | ||||
rs10484766 | 6 | 131578846 | intron variant | C/T | snv | 3.3E-02 | 4 |