Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1360780 | 0.708 | 0.320 | 6 | 35639794 | intron variant | T/A;C | snv | 31 | |||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
rs10767664 | 0.752 | 0.400 | 11 | 27704439 | intron variant | T/A | snv | 0.83 | 16 | ||
rs4906902 | 0.724 | 0.200 | 15 | 26774621 | intron variant | A/G | snv | 0.15 | 14 | ||
rs11030104 | 0.790 | 0.240 | 11 | 27662970 | intron variant | A/G | snv | 0.16 | 12 | ||
rs2283265 | 0.776 | 0.160 | 11 | 113414814 | intron variant | C/A | snv | 0.16 | 12 | ||
rs1076560 | 0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 | 11 | ||
rs7597593 | 0.827 | 0.160 | 2 | 184668853 | intron variant | T/C | snv | 0.53 | 6 | ||
rs10196867 | 0.925 | 0.080 | 2 | 79751234 | intron variant | C/G;T | snv | 5 | |||
rs1079597 | 0.827 | 0.080 | 11 | 113425564 | intron variant | C/T | snv | 0.18 | 5 | ||
rs147247472 | 0.925 | 0.080 | 1 | 49441901 | intron variant | G/A | snv | 7.3E-04 | 5 | ||
rs1534891 | 0.827 | 0.200 | 22 | 38299094 | intron variant | T/C | snv | 0.90 | 5 | ||
rs16917204 | 0.827 | 0.160 | 11 | 27646808 | intron variant | G/C | snv | 0.17 | 5 | ||
rs2133896 | 0.925 | 0.080 | 12 | 99455122 | intron variant | G/T | snv | 7.6E-02 | 5 | ||
rs6943555 | 0.882 | 0.080 | 7 | 70341037 | intron variant | T/A | snv | 0.34 | 5 | ||
rs884344 | 0.882 | 0.120 | 5 | 37824138 | intron variant | A/C | snv | 0.33 | 5 | ||
rs13306221 | 0.851 | 0.120 | 11 | 27701142 | intron variant | C/T | snv | 5.9E-02 | 4 | ||
rs11030096 | 0.925 | 0.160 | 11 | 27643996 | intron variant | T/A;C | snv | 3 | |||
rs2236861 | 0.882 | 0.080 | 1 | 28813244 | intron variant | G/A | snv | 0.19 | 3 | ||
rs1022563 | 0.925 | 0.080 | 20 | 1973693 | intron variant | C/G;T | snv | 2 | |||
rs1389752 | 0.925 | 0.080 | 9 | 13235288 | intron variant | A/G;T | snv | 2 | |||
rs1530351 | 0.925 | 0.080 | 17 | 65135491 | intron variant | G/A;C | snv | 2 | |||
rs1650420 | 1.000 | 0.080 | 16 | 10174473 | intron variant | T/C | snv | 0.58 | 2 | ||
rs16917234 | 0.925 | 0.080 | 11 | 27676827 | intron variant | T/A;C | snv | 2 | |||
rs1816071 | 0.925 | 0.080 | 5 | 161332949 | intron variant | T/C | snv | 0.37 | 2 |