Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10002268 | 1.000 | 0.080 | 4 | 55653725 | intergenic variant | T/C | snv | 0.41 | 1 | ||
rs10052657 | 0.807 | 0.120 | 5 | 59111944 | intron variant | C/A | snv | 0.17 | 7 | ||
rs10058728 | 1.000 | 0.080 | 5 | 149524529 | intron variant | A/T | snv | 0.64 | 2 | ||
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 53 | ||
rs1014867 | 0.925 | 0.080 | 4 | 125491736 | missense variant | C/T | snv | 4.9E-02 | 4.9E-02 | 3 | |
rs1035142 | 0.807 | 0.200 | 2 | 201288355 | 3 prime UTR variant | T/C;G | snv | 0.54 | 7 | ||
rs1039808 | 0.925 | 0.080 | 4 | 125318831 | missense variant | C/G;T | snv | 4.0E-06; 0.41 | 3 | ||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs1047972 | 0.716 | 0.240 | 20 | 56386407 | missense variant | T/C | snv | 0.85 | 0.84 | 19 | |
rs10484761 | 0.807 | 0.080 | 6 | 40834522 | intergenic variant | T/C | snv | 0.31 | 7 | ||
rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 71 | ||
rs104893819 | 0.827 | 0.240 | 3 | 30688470 | stop gained | C/G;T | snv | 5 | |||
rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 73 | |||
rs1048943 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 88 | |
rs10509670 | 0.851 | 0.080 | 10 | 94308190 | intron variant | A/G | snv | 0.30 | 5 | ||
rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs10786161 | 1.000 | 0.080 | 10 | 94347914 | intron variant | C/T | snv | 0.31 | 1 | ||
rs10821515 | 1.000 | 0.080 | 9 | 90862614 | intron variant | G/A;C | snv | 1 | |||
rs10842750 | 0.925 | 0.120 | 12 | 26537632 | intron variant | A/C;T | snv | 2 | |||
rs10882424 | 1.000 | 0.080 | 10 | 94326321 | intron variant | T/G | snv | 0.31 | 1 | ||
rs10882430 | 1.000 | 0.080 | 10 | 94330915 | 3 prime UTR variant | A/G | snv | 0.31 | 1 | ||
rs10931936 | 0.827 | 0.120 | 2 | 201279205 | intron variant | T/C | snv | 0.72 | 6 | ||
rs11066001 | 0.763 | 0.360 | 12 | 111681367 | intron variant | T/C | snv | 5.8E-03 | 15 |