Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs187238 | 0.602 | 0.680 | 11 | 112164265 | intron variant | C/A;G | snv | 48 | |||
rs1946518 | 0.602 | 0.760 | 11 | 112164735 | intron variant | T/G | snv | 0.60 | 46 | ||
rs755622 | 0.611 | 0.720 | 22 | 23894205 | intron variant | G/C | snv | 0.26 | 44 | ||
rs12203592 | 0.649 | 0.320 | 6 | 396321 | intron variant | C/T | snv | 0.10 | 38 | ||
rs180177035 | 0.752 | 0.280 | 7 | 140801502 | missense variant | T/C | snv | 35 | |||
rs104894226 | 0.658 | 0.560 | 11 | 534285 | missense variant | C/A;G;T | snv | 29 | |||
rs2740574 | 0.807 | 0.360 | 7 | 99784473 | upstream gene variant | C/T | snv | 0.78 | 12 | ||
rs2294020 | 0.763 | 0.280 | X | 49246763 | missense variant | A/G;T | snv | 10 | |||
rs5934505 | 0.776 | 0.120 | X | 8945785 | intergenic variant | T/A;C | snv | 10 | |||
rs1057517491 | 0.776 | 0.240 | 13 | 20189448 | frameshift variant | C/- | delins | 8 | |||
rs10502861 | 0.807 | 0.080 | 18 | 45220183 | intron variant | C/T | snv | 0.32 | 7 | ||
rs10888690 | 0.807 | 0.080 | 1 | 50494849 | intron variant | T/A;C | snv | 7 | |||
rs10930758 | 0.807 | 0.080 | 2 | 176897100 | intergenic variant | A/G;T | snv | 7 | |||
rs11037975 | 0.807 | 0.080 | 11 | 44389312 | intergenic variant | C/A;G | snv | 7 | |||
rs111668293 | 0.807 | 0.080 | 1 | 118896200 | intron variant | G/- | del | 0.12 | 7 | ||
rs115182912 | 0.807 | 0.080 | 3 | 126274431 | intron variant | G/A | snv | 1.5E-02 | 7 | ||
rs11593840 | 0.807 | 0.080 | 10 | 76436854 | intron variant | A/G | snv | 0.40 | 7 | ||
rs1160312 | 0.807 | 0.080 | 20 | 22069865 | intron variant | A/G | snv | 0.55 | 7 | ||
rs11684254 | 0.807 | 0.080 | 2 | 238787252 | downstream gene variant | C/G | snv | 0.44 | 7 | ||
rs12083887 | 0.807 | 0.080 | 1 | 118339066 | regulatory region variant | A/G | snv | 0.62 | 7 | ||
rs12214131 | 0.807 | 0.080 | 6 | 105760046 | intron variant | G/A | snv | 0.29 | 7 | ||
rs12565727 | 0.807 | 0.080 | 1 | 10973025 | intron variant | A/G | snv | 0.31 | 7 | ||
rs1262557 | 0.807 | 0.080 | 6 | 126733443 | intron variant | C/T | snv | 0.51 | 7 | ||
rs12702271 | 0.807 | 0.080 | 7 | 46904161 | intron variant | C/T | snv | 0.20 | 7 | ||
rs12902958 | 0.807 | 0.080 | 15 | 69747915 | intron variant | G/A | snv | 7.7E-02 | 7 |