Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10034228 | 0.882 | 0.040 | 4 | 111690594 | intergenic variant | T/C | snv | 0.32 | 1 | ||
rs10113215 | 1.000 | 0.040 | 8 | 59219635 | intergenic variant | A/G | snv | 0.33 | 1 | ||
rs10512441 | 1.000 | 0.040 | 17 | 32912627 | regulatory region variant | C/T | snv | 0.21 | 1 | ||
rs11658305 | 1.000 | 0.040 | 17 | 7526004 | intergenic variant | A/C;T | snv | 1 | |||
rs1370156 | 1.000 | 0.040 | 15 | 34692682 | intergenic variant | G/C | snv | 0.67 | 1 | ||
rs1556867 | 1.000 | 0.040 | 1 | 164244449 | intergenic variant | C/T | snv | 0.24 | 1 | ||
rs4373767 | 0.882 | 0.040 | 1 | 219586340 | regulatory region variant | C/T | snv | 0.32 | 1 | ||
rs61049169 | 1.000 | 0.040 | 2 | 146131140 | intergenic variant | G/A;C | snv | 1 | |||
rs73157695 | 1.000 | 0.040 | 21 | 45952033 | intergenic variant | G/A | snv | 0.29 | 1 | ||
rs9585327 | 1.000 | 0.040 | 13 | 100037100 | intergenic variant | G/A | snv | 0.36 | 1 | ||
rs8027411 | 0.882 | 0.040 | 15 | 79168687 | intron variant | G/T | snv | 0.52 | 1 | ||
rs7162310 | 1.000 | 0.040 | 15 | 63279035 | intron variant | C/T | snv | 0.28 | 1 | ||
rs4948523 | 1.000 | 0.040 | 10 | 58579338 | intron variant | A/C | snv | 0.51 | 1 | ||
rs5022942 | 1.000 | 0.040 | 4 | 81038812 | intron variant | A/G | snv | 0.59 | 1 | ||
rs5442 | 0.925 | 0.120 | 12 | 6845700 | missense variant | G/A | snv | 4.8E-02 | 4.6E-02 | 1 | |
rs34016308 | 1.000 | 0.040 | 14 | 92149397 | intron variant | -/TA | delins | 0.19 | 1 | ||
rs397515624 | 0.851 | 0.040 | 21 | 43169133 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs2155413 | 1.000 | 0.040 | 11 | 84923746 | intron variant | C/A | snv | 0.55 | 1 | ||
rs10892173 | 1.000 | 0.040 | 11 | 117801846 | 3 prime UTR variant | C/T | snv | 0.38 | 1 | ||
rs201140091 | 1.000 | 0.040 | 10 | 48200198 | intron variant | A/-;AAAAA;AAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAA;AAAAAAAAAAAAAA | delins | 1 | |||
rs297589 | 1.000 | 0.040 | 2 | 156502238 | intron variant | T/A | snv | 0.65 | 1 | ||
rs71041628 | 1.000 | 0.040 | 11 | 105794433 | intron variant | GTGTGTGTGT/-;GTGT;GTGTGT;GTGTGTGT;GTGTGTGTGTGT | delins | 0.67 | 1 | ||
rs10824518 | 0.882 | 0.040 | 10 | 77303784 | intron variant | T/A;C | snv | 1 | |||
rs2808510 | 1.000 | 0.040 | 1 | 200366947 | non coding transcript exon variant | C/T | snv | 0.29 | 1 | ||
rs2342406 | 1.000 | 0.040 | 2 | 44925609 | intron variant | T/C | snv | 0.19 | 1 |