Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 45 | |
rs11136000 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 19 | ||
rs3764650 | 0.790 | 0.200 | 19 | 1046521 | intron variant | T/G | snv | 0.14 | 9 | ||
rs11767557 | 0.882 | 0.080 | 7 | 143412046 | intron variant | T/C | snv | 0.18 | 4 | ||
rs2736990 | 0.882 | 0.080 | 4 | 89757390 | intron variant | G/A;T | snv | 4 | |||
rs12817488 | 1.000 | 0.040 | 12 | 122811747 | intron variant | G/A | snv | 0.39 | 3 | ||
rs597668 | 0.925 | 0.080 | 19 | 45205630 | intron variant | T/A;C;G | snv | 3 | |||
rs670139 | 0.925 | 0.080 | 11 | 60204322 | intron variant | G/A;T | snv | 3 | |||
rs10509125 | 10 | 60167108 | intron variant | C/A | snv | 0.56 | 2 | ||||
rs10994443 | 1.000 | 0.040 | 10 | 60635760 | intron variant | G/A | snv | 0.11 | 2 | ||
rs12734001 | 1.000 | 0.080 | 1 | 202421786 | intron variant | C/T | snv | 3.5E-05 | 2 | ||
rs1994090 | 1.000 | 0.040 | 12 | 40034759 | intron variant | G/A;T | snv | 2 | |||
rs4538475 | 1.000 | 0.040 | 4 | 15736314 | intron variant | A/G | snv | 0.24 | 2 | ||
rs6107516 | 1.000 | 0.120 | 20 | 4696446 | intron variant | G/A | snv | 0.23 | 2 | ||
rs9349407 | 1.000 | 0.080 | 6 | 47485642 | intron variant | G/C | snv | 0.23 | 2 | ||
rs1016726 | 7 | 29316787 | intron variant | G/A | snv | 0.12 | 1 | ||||
rs2756271 | 20 | 4684616 | intron variant | A/G;T | snv | 1 | |||||
rs6052751 | 20 | 4664427 | intron variant | G/A;C | snv | 1 | |||||
rs767181086 | 0.827 | 0.240 | 1 | 183220922 | stop gained | G/A;T | snv | 8.0E-06; 4.0E-06 | 11 | ||
rs80356711 | 1.000 | 20 | 4699698 | stop gained | C/T | snv | 4 | ||||
rs398122414 | 0.925 | 0.120 | 20 | 4699898 | stop gained | C/A | snv | 3 | |||
rs80356710 | 0.925 | 0.040 | 20 | 4699655 | stop gained | T/G | snv | 3 | |||
rs74315401 | 0.683 | 0.320 | 20 | 4699525 | missense variant | C/T | snv | 32 | |||
rs28933385 | 0.695 | 0.320 | 20 | 4699818 | missense variant | G/A | snv | 4.0E-06 | 25 | ||
rs1799990 | 0.683 | 0.440 | 20 | 4699605 | missense variant | A/G | snv | 0.31 | 0.33 | 23 |