Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1015362 | 0.925 | 0.080 | 20 | 34150806 | regulatory region variant | C/T | snv | 0.42 | 3 | ||
rs1015363 | 1.000 | 0.040 | 20 | 34150529 | intergenic variant | G/A | snv | 0.69 | 1 | ||
rs10231520 | 1.000 | 0.040 | 7 | 20742471 | intron variant | C/T | snv | 0.29 | 1 | ||
rs1024708183 | 0.925 | 0.040 | 19 | 7909761 | missense variant | A/G | snv | 4 | |||
rs1034265990 | 0.925 | 0.120 | 9 | 21971123 | missense variant | G/A;T | snv | 4.4E-06 | 2 | ||
rs1035142 | 0.807 | 0.200 | 2 | 201288355 | 3 prime UTR variant | T/C;G | snv | 0.54 | 7 | ||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs104894094 | 0.763 | 0.200 | 9 | 21971058 | missense variant | C/A;G;T | snv | 8.5E-06; 4.3E-06 | 12 | ||
rs104894095 | 0.827 | 0.120 | 9 | 21971200 | missense variant | C/G;T | snv | 9.0E-06 | 6 | ||
rs104894097 | 0.807 | 0.240 | 9 | 21974757 | missense variant | C/A;G;T | snv | 1.7E-05; 1.3E-05 | 8 | ||
rs104894098 | 0.851 | 0.200 | 9 | 21970982 | missense variant | A/T | snv | 5 | |||
rs104894099 | 0.851 | 0.200 | 9 | 21971183 | missense variant | A/C;T | snv | 4.6E-06 | 5 | ||
rs104894104 | 0.790 | 0.160 | 9 | 21971019 | missense variant | G/A;T | snv | 7 | |||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 73 | |||
rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 73 | |||
rs104894340 | 0.827 | 0.200 | 12 | 57751647 | missense variant | C/A;T | snv | 5 | |||
rs10492396 | 0.925 | 0.080 | 13 | 32384750 | non coding transcript exon variant | G/A | snv | 4.8E-02 | 2 | ||
rs10515789 | 1.000 | 0.040 | 5 | 159079407 | intron variant | T/G | snv | 0.11 | 1 | ||
rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 43 | |
rs1051849 | 1.000 | 0.040 | 17 | 37513222 | 3 prime UTR variant | T/C | snv | 9.9E-02 | 1 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs1057519695 | 0.641 | 0.520 | 1 | 114713907 | missense variant | TT/CA;CC | mnv | 35 | |||
rs1057519702 | 1.000 | 0.040 | 4 | 54726020 | missense variant | T/C | snv | 2 | |||
rs1057519703 | 1.000 | 0.040 | 4 | 54727418 | missense variant | A/C;T | snv | 1 | |||
rs1057519704 | 0.882 | 0.080 | 4 | 54727425 | missense variant | T/A | snv | 3 |