Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1154988 | 3 | 136206349 | upstream gene variant | T/A | snv | 0.76 | 7 | ||||
rs13108218 | 4 | 3442204 | intron variant | A/G;T | snv | 7 | |||||
rs10409243 | 19 | 10222312 | 3 prime UTR variant | C/A;G;T | snv | 6 | |||||
rs127430 | 20 | 58589799 | intron variant | A/G;T | snv | 6 | |||||
rs13125101 | 4 | 80253438 | TF binding site variant | G/A | snv | 0.24 | 6 | ||||
rs1887320 | 20 | 10985350 | intron variant | G/A | snv | 0.46 | 6 | ||||
rs2643826 | 3 | 27521497 | upstream gene variant | C/T | snv | 0.56 | 6 | ||||
rs415895 | 11 | 9748015 | missense variant | C/G | snv | 0.62 | 0.61 | 6 | |||
rs72681869 | 14 | 50188639 | missense variant | G/A;C | snv | 4.0E-06; 4.1E-03 | 6 | ||||
rs7890572 | X | 29622701 | intron variant | A/G | snv | 9.3E-02 | 6 | ||||
rs10059884 | 5 | 32832368 | regulatory region variant | C/A;T | snv | 5 | |||||
rs12258967 | 10 | 18439030 | intron variant | C/G;T | snv | 5 | |||||
rs12978472 | 19 | 7257979 | intron variant | C/G;T | snv | 5 | |||||
rs167479 | 19 | 11416089 | missense variant | T/A;C;G | snv | 5 | |||||
rs1894400 | 15 | 90885725 | intron variant | C/T | snv | 0.28 | 5 | ||||
rs3790604 | 1 | 112504257 | intron variant | C/A | snv | 7.8E-02 | 5 | ||||
rs62434109 | 6 | 150654176 | intron variant | T/G | snv | 8.4E-02 | 5 | ||||
rs7125196 | 11 | 61505093 | intron variant | T/C | snv | 0.16 | 5 | ||||
rs7246865 | 19 | 17108295 | intron variant | G/A | snv | 0.36 | 5 | ||||
rs1063857 | 12 | 6044348 | synonymous variant | A/G | snv | 0.31 | 0.40 | 4 | |||
rs10769254 | 11 | 47340914 | intron variant | G/C | snv | 0.27 | 4 | ||||
rs139491786 | 16 | 2036420 | missense variant | C/T | snv | 3.4E-03 | 3.5E-03 | 4 | |||
rs17725246 | 7 | 44542387 | upstream gene variant | T/A;C | snv | 4 | |||||
rs34042070 | 16 | 72067626 | intron variant | C/G | snv | 0.17 | 4 | ||||
rs3735533 | 7 | 27206274 | non coding transcript exon variant | T/C | snv | 0.93 | 4 |