Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
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 | ||
rs401681 | 0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 | 42 | ||
rs920778 | 0.633 | 0.480 | 12 | 53966448 | intron variant | G/A | snv | 0.57 | 36 | ||
rs12212067 | 0.716 | 0.320 | 6 | 108659993 | intron variant | T/G | snv | 0.14 | 20 | ||
rs2424913 | 0.708 | 0.440 | 20 | 32786453 | intron variant | C/T | snv | 0.56 | 0.53 | 18 | |
rs2494938 | 0.752 | 0.240 | 6 | 40568389 | intron variant | G/A | snv | 0.51 | 11 | ||
rs6898743 | 0.776 | 0.160 | 5 | 42602390 | intron variant | C/G | snv | 0.78 | 9 | ||
rs4767364 | 0.807 | 0.160 | 12 | 112083644 | intron variant | G/A | snv | 0.45 | 8 | ||
rs2285947 | 0.807 | 0.120 | 7 | 21544470 | intron variant | G/A | snv | 0.44 | 7 | ||
rs2014300 | 0.851 | 0.080 | 21 | 34985564 | intron variant | A/G;T | snv | 0.75 | 5 | ||
rs10950641 | 0.925 | 0.040 | 7 | 2294751 | intron variant | G/A | snv | 2.9E-02 | 4 | ||
rs11016879 | 0.882 | 0.040 | 10 | 129691518 | intron variant | A/C;G | snv | 0.66 | 4 | ||
rs4775319 | 0.925 | 0.040 | 15 | 60921365 | intron variant | G/A | snv | 0.62 | 4 | ||
rs6796803 | 0.925 | 0.040 | 3 | 186746318 | intron variant | T/A;C | snv | 4 | |||
rs11752942 | 0.882 | 0.080 | 6 | 40354019 | intron variant | A/G | snv | 0.46 | 3 | ||
rs522962 | 0.925 | 0.040 | 20 | 49526825 | intron variant | T/C | snv | 0.61 | 2 | ||
rs6019902 | 0.925 | 0.040 | 20 | 49561676 | intron variant | G/A | snv | 0.21 | 2 | ||
rs6125671 | 0.925 | 0.040 | 20 | 49559061 | intron variant | C/T | snv | 0.24 | 2 | ||
rs6598072 | 0.925 | 0.040 | 11 | 219793 | intron variant | C/T | snv | 0.79 | 2 | ||
rs7802034 | 0.925 | 0.040 | 7 | 152655183 | intron variant | A/C;G | snv | 2 | |||
rs927068 | 0.925 | 0.040 | 20 | 49561437 | intron variant | G/T | snv | 0.32 | 2 | ||
rs10484761 | 0.807 | 0.080 | 6 | 40834522 | intergenic variant | T/C | snv | 0.31 | 7 | ||
rs1667255 | 0.925 | 0.040 | 18 | 31607316 | intergenic variant | A/C;G;T | snv | 3 |