Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1047303 | 0.851 | 0.120 | 1 | 119514623 | missense variant | C/A | snv | 0.75 | 4 | ||
rs1047768 | 0.695 | 0.320 | 13 | 102852167 | synonymous variant | T/C | snv | 0.52 | 0.59 | 20 | |
rs1047840 | 0.708 | 0.280 | 1 | 241878999 | missense variant | G/A | snv | 0.36 | 0.40 | 19 | |
rs10483813 | 0.851 | 0.120 | 14 | 68564567 | intron variant | T/A;C | snv | 4 | |||
rs10486567 | 0.851 | 0.120 | 7 | 27936944 | intron variant | G/A | snv | 0.28 | 9 | ||
rs1048943 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 88 | |
rs1049216 | 0.790 | 0.200 | 4 | 184628935 | 3 prime UTR variant | A/G | snv | 0.27 | 9 | ||
rs10503733 | 0.925 | 0.080 | 8 | 23676505 | downstream gene variant | G/T | snv | 0.27 | 2 | ||
rs1050450 | 0.623 | 0.600 | 3 | 49357401 | missense variant | G/A | snv | 0.28 | 0.30 | 43 | |
rs10505346 | 0.925 | 0.080 | 8 | 118951604 | intron variant | G/T | snv | 0.22 | 4 | ||
rs10505474 | 0.925 | 0.080 | 8 | 127405259 | intron variant | T/C | snv | 0.47 | 3 | ||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 31 | ||
rs10505483 | 0.925 | 0.080 | 8 | 127112950 | intron variant | C/T | snv | 0.16 | 2 | ||
rs10519097 | 0.708 | 0.320 | 15 | 60997989 | intron variant | C/T | snv | 0.13 | 18 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs1052576 | 0.807 | 0.200 | 1 | 15506048 | missense variant | T/A;C | snv | 0.53 | 9 | ||
rs1056827 | 0.683 | 0.400 | 2 | 38075034 | missense variant | C/A | snv | 0.32 | 0.35 | 24 | |
rs1056836 | 0.581 | 0.680 | 2 | 38071060 | missense variant | G/C | snv | 0.51 | 58 | ||
rs1057519864 | 0.851 | 0.080 | X | 67723707 | missense variant | T/C | snv | 8 | |||
rs1057519912 | 0.776 | 0.200 | X | 71129408 | missense variant | C/G;T | snv | 11 | |||
rs1057519966 | 0.882 | 0.080 | 17 | 49619064 | missense variant | A/C;T | snv | 3 | |||
rs1057519972 | 0.882 | 0.080 | 17 | 49619327 | missense variant | A/T | snv | 3 | |||
rs1057520005 | 0.742 | 0.360 | 17 | 7673800 | missense variant | C/A;G | snv | 14 | |||
rs1058205 | 0.925 | 0.080 | 19 | 50860142 | 3 prime UTR variant | C/T | snv | 0.75 | 0.74 | 3 | |
rs1058587 | 0.882 | 0.200 | 19 | 18388612 | missense variant | C/G;T | snv | 0.24; 9.1E-06 | 4 |