Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1544410 | 0.542 | 0.760 | 12 | 47846052 | intron variant | C/A;G;T | snv | 78 | |||
rs2234693 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 77 | ||
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 59 | ||
rs7975232 | 0.576 | 0.760 | 12 | 47845054 | intron variant | C/A | snv | 0.51 | 0.55 | 56 | |
rs755622 | 0.611 | 0.720 | 22 | 23894205 | intron variant | G/C | snv | 0.26 | 44 | ||
rs13277113 | 0.695 | 0.520 | 8 | 11491677 | intron variant | G/A | snv | 0.25 | 18 | ||
rs2670660 | 0.708 | 0.400 | 17 | 5615686 | intron variant | A/G | snv | 0.41 | 15 | ||
rs10036748 | 0.752 | 0.360 | 5 | 151078585 | intron variant | C/A;T | snv | 11 | |||
rs10499194 | 0.752 | 0.400 | 6 | 137681500 | intron variant | C/T | snv | 0.24 | 10 | ||
rs4958847 | 0.807 | 0.120 | 5 | 150860025 | intron variant | G/A | snv | 0.25 | 8 | ||
rs11747270 | 0.790 | 0.240 | 5 | 150879305 | intron variant | A/G | snv | 0.21 | 7 | ||
rs2248098 | 0.925 | 0.120 | 12 | 47859573 | intron variant | A/G;T | snv | 4 | |||
rs4760648 | 0.851 | 0.200 | 12 | 47886882 | intron variant | C/A;G;T | snv | 4 | |||
rs204991 | 0.882 | 0.200 | 6 | 32193589 | intron variant | T/C | snv | 0.21 | 3 | ||
rs3890733 | 0.882 | 0.120 | 12 | 47895590 | intron variant | C/T | snv | 0.27 | 3 | ||
rs10911363 | 0.925 | 0.120 | 1 | 183580622 | intron variant | G/T | snv | 0.30 | 2 | ||
rs11168268 | 0.925 | 0.120 | 12 | 47858029 | intron variant | G/A | snv | 0.57 | 2 | ||
rs204989 | 0.925 | 0.120 | 6 | 32194075 | intron variant | G/A | snv | 0.21 | 2 | ||
rs2165667 | 0.925 | 0.040 | 4 | 186540475 | intron variant | A/G;T | snv | 2 | |||
rs540558 | 0.925 | 0.120 | 5 | 38844171 | intron variant | C/G | snv | 0.19 | 2 | ||
rs7033979 | 0.925 | 0.040 | 9 | 92461698 | intron variant | A/G;T | snv | 2 | |||
rs6074028 | 1.000 | 0.040 | 20 | 46126219 | intron variant | A/C;G | snv | 1 | |||
rs73115010 | 1.000 | 0.040 | 20 | 46124597 | intron variant | T/C | snv | 0.18 | 1 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 |