Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1334496 | 1.000 | 0.040 | X | 137178554 | intergenic variant | C/A;T | snv | 1 | |||
rs4829605 | 1.000 | 0.040 | X | 137182822 | intergenic variant | C/A;G | snv | 1 | |||
rs11767557 | 0.882 | 0.080 | 7 | 143412046 | intron variant | T/C | snv | 0.18 | 4 | ||
rs111943087 | 0.925 | 0.080 | 5 | 150059725 | missense variant | G/A | snv | 1.4E-05 | 2 | ||
rs3756577 | 0.925 | 0.080 | 5 | 150249081 | intron variant | C/T | snv | 0.14 | 2 | ||
rs3822606 | 0.925 | 0.080 | 5 | 150261592 | intron variant | G/A | snv | 0.27 | 2 | ||
rs375752214 | 0.708 | 0.400 | 7 | 150998541 | missense variant | C/T | snv | 4.1E-06 | 4.2E-05 | 22 | |
rs9340803 | 0.925 | 0.080 | 6 | 151842832 | intron variant | A/G | snv | 1.0E-03 | 3.8E-04 | 2 | |
rs2230288 | 0.776 | 0.160 | 1 | 155236376 | missense variant | C/T | snv | 1.0E-02 | 1.0E-02 | 18 | |
rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
rs640476 | 1.000 | 0.040 | 5 | 161277998 | intergenic variant | T/G | snv | 0.42 | 1 | ||
rs6850306 | 0.925 | 0.080 | 4 | 18004466 | intron variant | G/A | snv | 0.12 | 2 | ||
rs12053868 | 0.925 | 0.080 | 3 | 190582215 | intron variant | A/G | snv | 8.0E-02 | 2 | ||
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs63750048 | 0.925 | 0.080 | 1 | 226883817 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs391300 | 0.882 | 0.160 | 17 | 2312964 | intron variant | T/C | snv | 0.58 | 4 | ||
rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
rs11887120 | 0.882 | 0.080 | 2 | 25262866 | intron variant | C/T | snv | 0.45 | 4 | ||
rs11136000 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 19 | ||
rs9331888 | 0.827 | 0.200 | 8 | 27611345 | 5 prime UTR variant | C/G | snv | 0.35 | 0.28 | 5 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs1451603364 | 0.925 | 0.120 | 11 | 27658411 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs2534672 | 1.000 | 0.040 | 6 | 31497781 | intron variant | G/C | snv | 0.32 | 1 | ||
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 |