Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1834306 | 0.776 | 0.200 | 11 | 122152479 | intron variant | A/G | snv | 0.49 | 9 | ||
rs2069845 | 0.807 | 0.120 | 7 | 22730530 | intron variant | G/A | snv | 0.61 | 8 | ||
rs2665390 | 0.776 | 0.160 | 3 | 156679960 | intron variant | C/T | snv | 0.92 | 8 | ||
rs3024971 | 0.827 | 0.200 | 12 | 57099944 | intron variant | T/G | snv | 7.8E-02 | 7.9E-02 | 7 | |
rs3176352 | 0.807 | 0.120 | 6 | 36684562 | intron variant | C/A;G;T | snv | 8.0E-06; 0.37; 2.0E-05 | 7 | ||
rs34214448 | 0.851 | 0.120 | 17 | 51154651 | intron variant | G/T | snv | 0.39 | 7 | ||
rs3765459 | 0.807 | 0.280 | 20 | 46128768 | intron variant | G/A;C | snv | 0.22 | 7 | ||
rs4851527 | 0.790 | 0.160 | 2 | 102005914 | intron variant | A/G | snv | 0.63 | 7 | ||
rs7372209 | 0.807 | 0.160 | 3 | 37969217 | intron variant | T/C | snv | 0.77 | 7 | ||
rs1266828 | 0.807 | 0.120 | 6 | 52243264 | intron variant | G/A | snv | 0.75 | 6 | ||
rs13117307 | 0.827 | 0.080 | 4 | 55885574 | intron variant | C/T | snv | 0.21 | 6 | ||
rs3218896 | 0.807 | 0.160 | 2 | 102015190 | intron variant | T/C;G | snv | 6 | |||
rs4282438 | 0.807 | 0.280 | 6 | 33104395 | intron variant | T/G | snv | 3.1E-02 | 6 | ||
rs4848320 | 0.807 | 0.120 | 2 | 113253214 | intron variant | C/G;T | snv | 6 | |||
rs1143630 | 0.827 | 0.160 | 2 | 112834078 | intron variant | T/A;G | snv | 5 | |||
rs11568785 | 0.882 | 0.080 | 9 | 99143552 | intron variant | A/G;T | snv | 7.2E-02 | 5 | ||
rs266085 | 0.851 | 0.200 | 10 | 44378805 | intron variant | C/T | snv | 0.32 | 5 | ||
rs3826392 | 0.827 | 0.200 | 17 | 12019587 | intron variant | G/T | snv | 0.65 | 5 | ||
rs719250 | 0.827 | 0.200 | 2 | 102007256 | intron variant | C/T | snv | 0.11 | 5 | ||
rs1007541 | 0.882 | 0.080 | 2 | 48981895 | intron variant | C/T | snv | 0.16 | 4 | ||
rs1474348 | 0.882 | 0.080 | 7 | 22728289 | intron variant | C/G | snv | 0.71 | 4 | ||
rs16970849 | 0.882 | 0.080 | 17 | 78137827 | intron variant | G/A;T | snv | 0.11; 4.0E-06 | 4 | ||
rs2289937 | 0.882 | 0.080 | 8 | 116861572 | intron variant | G/A;C | snv | 4 | |||
rs2290907 | 0.882 | 0.080 | 17 | 78097596 | intron variant | T/C | snv | 0.23 | 4 | ||
rs3809728 | 0.851 | 0.120 | 17 | 12019847 | intron variant | A/C;T | snv | 4 |