Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 93 | |||
rs1421085 | 0.752 | 0.280 | 16 | 53767042 | intron variant | T/C | snv | 0.31 | 28 | ||
rs2229616 | 0.732 | 0.200 | 18 | 60372043 | missense variant | C/T | snv | 1.6E-02 | 1.6E-02 | 22 | |
rs1558902 | 0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 | 21 | ||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 19 | ||
rs4988235 | 0.752 | 0.400 | 2 | 135851076 | intron variant | G/A;C | snv | 19 | |||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 17 | |||
rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 17 | ||
rs543874 | 1.000 | 0.080 | 1 | 177920345 | upstream gene variant | A/G | snv | 0.21 | 11 | ||
rs2112347 | 0.925 | 0.120 | 5 | 75719417 | upstream gene variant | T/G | snv | 0.42 | 10 | ||
rs3810291 | 19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 | 9 | ||||
rs12967135 | 18 | 60181790 | intergenic variant | G/A | snv | 0.24 | 8 | ||||
rs2820443 | 0.882 | 0.120 | 1 | 219580167 | regulatory region variant | T/C | snv | 0.23 | 8 | ||
rs1516725 | 0.925 | 0.120 | 3 | 186106215 | intron variant | T/C | snv | 0.86 | 8 | ||
rs6569648 | 1.000 | 0.080 | 6 | 130027974 | intron variant | C/T | snv | 0.84 | 7 | ||
rs12446632 | 1.000 | 0.080 | 16 | 19924067 | intergenic variant | G/A | snv | 0.11 | 7 | ||
rs7531118 | 1.000 | 0.080 | 1 | 72371556 | intron variant | T/C | snv | 0.40 | 7 | ||
rs10132280 | 14 | 25458973 | intergenic variant | C/A | snv | 0.37 | 6 | ||||
rs17391694 | 0.882 | 0.120 | 1 | 78157942 | regulatory region variant | C/T | snv | 7.8E-02 | 6 | ||
rs887912 | 1.000 | 0.080 | 2 | 59075742 | intron variant | T/C;G | snv | 6 | |||
rs806794 | 6 | 26200449 | 3 prime UTR variant | A/G | snv | 0.36 | 6 | ||||
rs12936587 | 0.882 | 0.080 | 17 | 17640408 | regulatory region variant | G/A | snv | 0.38 | 5 | ||
rs11676272 | 1.000 | 0.040 | 2 | 24918669 | missense variant | A/G | snv | 0.47 | 0.57 | 5 | |
rs113191842 | 16 | 53783406 | intron variant | G/A | snv | 9.4E-02 | 5 |