Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
rs1121980 | 0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv | 5 | |||
rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 9 | |||
rs11604424 | 11 | 116780399 | intron variant | C/G;T | snv | 3 | |||||
rs11652146 | 17 | 49345001 | intron variant | G/A;C | snv | 4 | |||||
rs11765979 | 7 | 130761118 | intergenic variant | A/C;G | snv | 2 | |||||
rs11870935 | 17 | 47655239 | intron variant | G/A;C | snv | 4 | |||||
rs11987974 | 8 | 36966299 | intergenic variant | C/A;T | snv | 4 | |||||
rs12225230 | 11 | 116857914 | missense variant | G/A;C;T | snv | 1.2E-05; 0.19; 4.0E-06 | 3 | ||||
rs127430 | 20 | 58589799 | intron variant | A/G;T | snv | 5 | |||||
rs13114738 | 0.851 | 0.120 | 4 | 102363708 | intron variant | C/A;T | snv | 16 | |||
rs13326165 | 3 | 52498102 | intron variant | A/G;T | snv | 2 | |||||
rs13702 | 0.925 | 0.160 | 8 | 19966981 | 3 prime UTR variant | T/A;C | snv | 2 | |||
rs148149124 | 15 | 43382233 | intron variant | TAAAAGAAAAA/-;TAAAAGAAAAATAAAAGAAAAA | delins | 2 | |||||
rs149580368 | 17 | 43797377 | downstream gene variant | C/A | snv | 2 | |||||
rs150090666 | 11 | 14843853 | stop gained | C/G;T | snv | 8.0E-06; 5.8E-04 | 2 | ||||
rs150844304 | 15 | 43434427 | intron variant | A/C;G | snv | 4 | |||||
rs1532085 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 7 | |||
rs1558861 | 11 | 116736721 | regulatory region variant | C/G;T | snv | 4 | |||||
rs1562398 | 7 | 130773172 | intergenic variant | C/G;T | snv | 2 | |||||
rs1565228 | 11 | 27564889 | intron variant | G/A;C | snv | 4 | |||||
rs17100926 | 14 | 71727684 | intron variant | C/A;T | snv | 2 | |||||
rs17199964 | 4 | 101786634 | intron variant | G/A;C | snv | 5 | |||||
rs17231506 | 0.851 | 0.040 | 16 | 56960616 | upstream gene variant | C/G;T | snv | 0.28 | 8 | ||
rs1728918 | 0.827 | 0.160 | 2 | 27412596 | upstream gene variant | A/G;T | snv | 18 |