Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1008563 | 1.000 | 0.080 | 2 | 218162165 | downstream gene variant | G/A | snv | 0.43 | 1 | ||
rs10176176 | 1.000 | 0.080 | 2 | 85534925 | upstream gene variant | A/T | snv | 0.54 | 1 | ||
rs17708087 | 1.000 | 0.080 | 17 | 40514261 | upstream gene variant | A/G | snv | 0.15 | 1 | ||
rs2019090 | 1.000 | 0.080 | 11 | 103798234 | intron variant | A/C;G;T | snv | 1 | |||
rs2315065 | 1.000 | 0.080 | 6 | 160687112 | intergenic variant | C/A;T | snv | 1 | |||
rs490556 | 1.000 | 0.080 | 5 | 4022536 | intergenic variant | G/A | snv | 0.57 | 1 | ||
rs521660 | 1.000 | 0.080 | 5 | 4035819 | intron variant | T/C | snv | 0.61 | 1 | ||
rs6941513 | 1.000 | 0.080 | 6 | 163609768 | intergenic variant | A/G | snv | 0.45 | 1 | ||
rs7211079 | 1.000 | 0.080 | 17 | 80133738 | downstream gene variant | A/G | snv | 0.29 | 1 | ||
rs822387 | 1.000 | 0.080 | 3 | 186838248 | upstream gene variant | T/C | snv | 0.15 | 1 | ||
rs13301354 | 1.000 | 0.080 | 9 | 137030185 | 3 prime UTR variant | T/C | snv | 0.64 | 1 | ||
rs9635480 | 1.000 | 0.080 | 16 | 16000744 | intron variant | A/G | snv | 0.50 | 1 | ||
rs6138473 | 1.000 | 0.080 | 20 | 25031519 | intron variant | C/T | snv | 0.38 | 1 | ||
rs2275725 | 1.000 | 0.080 | 10 | 133275531 | missense variant | A/G | snv | 0.89 | 0.90 | 1 | |
rs2995300 | 1.000 | 0.080 | 10 | 133263019 | 3 prime UTR variant | C/A | snv | 0.87 | 0.83 | 1 | |
rs72563731 | 1.000 | 0.080 | 3 | 186854292 | missense variant | C/T | snv | 1.6E-05 | 2.3E-04 | 1 | |
rs200741295 | 1.000 | 0.080 | 17 | 15975230 | missense variant | A/G;T | snv | 1.3E-04; 4.0E-06 | 7.0E-06 | 1 | |
rs761660984 | 1.000 | 0.080 | 3 | 186620589 | missense variant | G/A;C;T | snv | 2.9E-05 | 1 | ||
rs3803915 | 1.000 | 0.080 | 19 | 2160530 | intron variant | C/A;T | snv | 1 | |||
rs369066087 | 1.000 | 0.080 | 11 | 116837117 | synonymous variant | G/A;C | snv | 2.0E-05 | 2.8E-05 | 1 | |
rs1135402763 | 1.000 | 0.080 | 2 | 21032540 | missense variant | T/C;G | snv | 1 | |||
rs1275147925 | 1.000 | 0.080 | 19 | 44906613 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
rs1458301734 | 1.000 | 0.080 | 19 | 44908687 | missense variant | G/A;T | snv | 5.9E-06 | 1 | ||
rs868094551 | 1.000 | 0.080 | 19 | 44908768 | missense variant | C/A;T | snv | 1 | |||
rs17599586 | 1.000 | 0.080 | 6 | 131583579 | intron variant | C/T | snv | 0.11 | 1 |