Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10012 | 0.716 | 0.280 | 2 | 38075247 | missense variant | G/C | snv | 0.31 | 0.36 | 16 | |
rs1002481 | 0.882 | 0.080 | 6 | 111390819 | intron variant | T/A;G | snv | 3 | |||
rs10036653 | 0.851 | 0.160 | 5 | 81970563 | upstream gene variant | A/T | snv | 0.17 | 4 | ||
rs10040363 | 0.882 | 0.080 | 5 | 83177826 | intron variant | A/G | snv | 0.50 | 3 | ||
rs10053847 | 0.882 | 0.080 | 5 | 35878038 | 3 prime UTR variant | G/A | snv | 0.13 | 3 | ||
rs10054203 | 0.882 | 0.080 | 5 | 1279849 | intron variant | G/A;C;T | snv | 3 | |||
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 40 | ||
rs10079250 | 0.827 | 0.120 | 5 | 150070569 | missense variant | T/C | snv | 9.9E-02 | 8.6E-02 | 7 | |
rs1014264982 | 0.882 | 0.080 | 19 | 3577038 | missense variant | G/A;C | snv | 6.8E-06 | 7.0E-06 | 3 | |
rs10187911 | 0.882 | 0.080 | 2 | 50420809 | intron variant | C/A;G;T | snv | 3 | |||
rs1019340046 | 0.882 | 0.080 | 17 | 7674225 | missense variant | C/T | snv | 4 | |||
rs10213865 | 0.827 | 0.120 | 5 | 35857748 | intron variant | A/C;T | snv | 5 | |||
rs10244817 | 0.882 | 0.080 | 7 | 124827416 | intron variant | T/C | snv | 0.22 | 3 | ||
rs10254120 | 0.851 | 0.080 | 7 | 6005996 | missense variant | C/A;G;T | snv | 7.2E-02 | 5 | ||
rs1026411 | 0.827 | 0.080 | 8 | 127014165 | intron variant | G/A;C | snv | 0.25 | 5 | ||
rs1035938 | 0.776 | 0.120 | 19 | 47680514 | missense variant | C/G;T | snv | 0.29 | 8 | ||
rs10412613 | 0.882 | 0.080 | 19 | 52209575 | intron variant | G/A | snv | 0.63 | 3 | ||
rs1041983 | 0.732 | 0.240 | 8 | 18400285 | synonymous variant | C/T | snv | 0.34 | 0.36 | 15 | |
rs1042028 | 0.658 | 0.440 | 16 | 28606193 | missense variant | C/T | snv | 0.22 | 0.30 | 30 | |
rs10421768 | 0.807 | 0.120 | 19 | 35281996 | intron variant | A/G | snv | 0.21 | 6 | ||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1042711 | 0.827 | 0.120 | 5 | 148826785 | 5 prime UTR variant | C/A;G;T | snv | 4.2E-06; 0.68 | 5 | ||
rs1043973338 | 0.882 | 0.080 | 2 | 112830483 | missense variant | A/C | snv | 3 | |||
rs1043994 | 0.827 | 0.120 | 19 | 15192033 | synonymous variant | T/A;C | snv | 4.0E-06; 0.85 | 7 | ||
rs1044396 | 0.742 | 0.240 | 20 | 63349782 | missense variant | G/A;C | snv | 0.47; 6.1E-05 | 17 |