Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs765803011 | 1.000 | 0.040 | 16 | 27363094 | missense variant | C/G;T | snv | 4.0E-06; 1.6E-05 | 1 | ||
rs2920283 | 0.925 | 0.040 | 8 | 142675619 | intron variant | T/C | snv | 0.44 | 2 | ||
rs9315542 | 1.000 | 0.040 | 13 | 38057334 | intron variant | T/C | snv | 0.26 | 1 | ||
rs61516247 | 1.000 | 0.040 | 6 | 40344500 | non coding transcript exon variant | G/A | snv | 0.17 | 1 | ||
rs6672420 | 0.827 | 0.120 | 1 | 24964519 | missense variant | A/T | snv | 0.56 | 0.50 | 6 | |
rs1440526066 | 1.000 | 0.040 | 5 | 132679827 | missense variant | G/A | snv | 1 | |||
rs629367 | 0.776 | 0.200 | 11 | 122146306 | intron variant | C/A | snv | 0.88 | 11 | ||
rs6939861 | 0.882 | 0.080 | 6 | 41735303 | intron variant | G/A | snv | 0.24 | 3 | ||
rs895819 | 0.623 | 0.560 | 19 | 13836478 | non coding transcript exon variant | T/A;C;G | snv | 0.34 | 0.38 | 46 | |
rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
rs121224 | 0.851 | 0.080 | 17 | 31574981 | intron variant | G/C | snv | 0.66 | 4 | ||
rs7521584 | 1.000 | 0.040 | 1 | 1168578 | upstream gene variant | T/A;G | snv | 3 | |||
rs10739971 | 0.882 | 0.080 | 9 | 94175398 | intron variant | G/A;C | snv | 5 | |||
rs8111742 | 0.851 | 0.120 | 19 | 51692221 | intron variant | G/A;C | snv | 0.30 | 4 | ||
rs17276588 | 0.882 | 0.120 | X | 53557457 | intron variant | G/A | snv | 9.0E-02 | 4.2E-02 | 4 | |
rs2014486 | 1.000 | 0.040 | 11 | 1237573 | intron variant | A/G | snv | 0.52 | 2 | ||
rs7481521 | 1.000 | 0.040 | 11 | 1027811 | missense variant | C/T | snv | 0.50 | 0.47 | 1 | |
rs158916 | 0.882 | 0.080 | 5 | 60949318 | intron variant | A/G | snv | 0.15 | 3 | ||
rs2297518 | 0.658 | 0.480 | 17 | 27769571 | missense variant | G/A | snv | 0.18 | 0.17 | 30 | |
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs9471643 | 0.882 | 0.080 | 6 | 41751177 | intron variant | G/C | snv | 0.19 | 6 | ||
rs6458238 | 0.882 | 0.080 | 6 | 41749967 | intron variant | G/A;C | snv | 4 | |||
rs3789210 | 0.882 | 0.080 | 6 | 41743584 | intron variant | C/G;T | snv | 3 | |||
rs4711690 | 0.882 | 0.080 | 6 | 41741200 | missense variant | C/G | snv | 0.19 | 0.20 | 3 | |
rs6912200 | 0.925 | 0.080 | 6 | 41750170 | intron variant | C/T | snv | 0.54 | 3 |