Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1044129 | 0.790 | 0.200 | 15 | 33866065 | 3 prime UTR variant | A/G;T | snv | 9 | |||
rs1044484322 | 0.925 | 0.080 | 2 | 201271565 | missense variant | T/A;G | snv | 4.0E-06 | 2 | ||
rs1045012 | 0.925 | 0.080 | 7 | 99386731 | missense variant | G/C | snv | 5.6E-02 | 7.8E-02 | 2 | |
rs1045411 | 0.708 | 0.360 | 13 | 30459095 | 3 prime UTR variant | C/T | snv | 0.20 | 16 | ||
rs1045485 | 0.637 | 0.480 | 2 | 201284866 | missense variant | G/A;C;T | snv | 4.0E-06; 9.0E-02 | 34 | ||
rs1045494 | 0.882 | 0.120 | 2 | 201287058 | 3 prime UTR variant | T/C | snv | 0.10 | 3 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs10462028 | 0.882 | 0.120 | 4 | 55432133 | 3 prime UTR variant | G/A | snv | 0.28 | 3 | ||
rs10463297 | 0.925 | 0.080 | 5 | 140556654 | intron variant | T/C | snv | 0.29 | 2 | ||
rs1046428 | 0.776 | 0.200 | 14 | 77327940 | missense variant | T/A;C | snv | 4.0E-06; 0.81 | 8 | ||
rs10474352 | 0.925 | 0.080 | 5 | 91436408 | intron variant | C/T | snv | 0.23 | 2 | ||
rs10477313 | 0.925 | 0.080 | 5 | 146854076 | intron variant | C/T | snv | 0.17 | 2 | ||
rs1047768 | 0.695 | 0.320 | 13 | 102852167 | synonymous variant | T/C | snv | 0.52 | 0.59 | 20 | |
rs1047769 | 0.925 | 0.080 | 13 | 102861594 | missense variant | A/G | snv | 3.0E-02 | 2.5E-02 | 2 | |
rs1047840 | 0.708 | 0.280 | 1 | 241878999 | missense variant | G/A | snv | 0.36 | 0.40 | 19 | |
rs1047972 | 0.716 | 0.240 | 20 | 56386407 | missense variant | T/C | snv | 0.85 | 0.84 | 19 | |
rs1048108 | 0.827 | 0.120 | 2 | 214809500 | missense variant | G/A | snv | 0.38 | 0.33 | 5 | |
rs1048249612 | 0.925 | 0.080 | 11 | 125629291 | missense variant | G/A | snv | 2 | |||
rs10483028 | 0.925 | 0.080 | 21 | 35301275 | intron variant | C/T | snv | 0.18 | 2 | ||
rs10483813 | 0.851 | 0.120 | 14 | 68564567 | intron variant | T/A;C | snv | 4 | |||
rs10484919 | 0.925 | 0.080 | 6 | 151653287 | upstream gene variant | C/T | snv | 0.16 | 2 | ||
rs10485805 | 0.925 | 0.080 | 20 | 56370727 | intron variant | A/G | snv | 0.23 | 2 | ||
rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 43 | ||
rs1048943 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 88 | |
rs1048945 | 0.851 | 0.120 | 14 | 20456008 | missense variant | G/C | snv | 2.1E-02 | 2.4E-02 | 6 |