Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs28933979 | 0.587 | 0.600 | 18 | 31592974 | missense variant | G/A;C | snv | 1.0E-04 | 70 | ||
rs6277 | 0.689 | 0.480 | 11 | 113412737 | synonymous variant | G/A | snv | 0.41 | 0.38 | 36 | |
rs121918457 | 0.701 | 0.280 | 12 | 112488466 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 24 | |
rs6746030 | 0.763 | 0.320 | 2 | 166242648 | missense variant | A/G | snv | 0.88 | 0.88 | 16 | |
rs8065080 | 0.827 | 0.200 | 17 | 3577153 | missense variant | T/C | snv | 0.37 | 0.32 | 11 | |
rs1800866 | 0.851 | 0.080 | 9 | 34637693 | missense variant | T/G | snv | 0.20 | 0.18 | 8 | |
rs6796803 | 0.925 | 0.040 | 3 | 186746318 | intron variant | T/A;C | snv | 4 | |||
rs4775319 | 0.925 | 0.040 | 15 | 60921365 | intron variant | G/A | snv | 0.62 | 4 | ||
rs10950641 | 0.925 | 0.040 | 7 | 2294751 | intron variant | G/A | snv | 2.9E-02 | 4 | ||
rs104894851 | 0.925 | 0.200 | X | 101398920 | stop gained | G/T | snv | 3 | |||
rs104894852 | 0.925 | 0.200 | X | 101397871 | missense variant | T/C | snv | 3 | |||
rs4804217 | 1.000 | 0.040 | 19 | 7634461 | intron variant | C/T | snv | 0.29 | 3 | ||
rs1017715903 | 1.000 | 0.080 | 1 | 161306854 | stop gained | C/T | snv | 2 | |||
rs10814130 | 9 | 34637994 | upstream gene variant | C/A | snv | 0.17 | 1 |