Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1409313 | 1.000 | 0.040 | 10 | 102431844 | intron variant | T/C | snv | 0.85 | 1 | ||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 5 | ||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 10 | ||
rs4773054 | 1.000 | 0.040 | 13 | 109501681 | intron variant | T/C | snv | 0.89 | 2 | ||
rs6537825 | 1.000 | 0.040 | 1 | 114405659 | missense variant | A/G | snv | 0.88 | 0.92 | 1 | |
rs11582563 | 1.000 | 0.040 | 1 | 114416918 | intron variant | G/A | snv | 0.14 | 1 | ||
rs11585926 | 1.000 | 0.040 | 1 | 114431068 | intron variant | T/C | snv | 0.22 | 3 | ||
rs11589568 | 1.000 | 0.040 | 1 | 114453702 | intron variant | T/C | snv | 0.14 | 1 | ||
rs7511633 | 1.000 | 0.040 | 1 | 114456655 | intron variant | G/A | snv | 0.36 | 1 | ||
rs6661053 | 1.000 | 0.040 | 1 | 114496497 | intron variant | T/A;C | snv | 1 | |||
rs11102800 | 1.000 | 0.040 | 1 | 114498310 | intron variant | C/T | snv | 0.58 | 2 | ||
rs3827735 | 1.000 | 0.040 | 1 | 114510087 | intron variant | C/A;T | snv | 1 | |||
rs11102807 | 1.000 | 0.040 | 1 | 114518963 | intergenic variant | A/G | snv | 0.44 | 1 | ||
rs10858047 | 1.000 | 0.040 | 1 | 114531255 | upstream gene variant | T/C | snv | 0.13 | 1 | ||
rs11587400 | 1.000 | 0.040 | 1 | 114537037 | non coding transcript exon variant | C/G;T | snv | 1 | |||
rs1877455 | 1.000 | 0.040 | 1 | 114556471 | intergenic variant | C/T | snv | 0.12 | 1 | ||
rs926938 | 1.000 | 0.040 | 1 | 114697195 | upstream gene variant | A/G;T | snv | 1 | |||
rs8453 | 1.000 | 0.040 | 1 | 114716978 | 3 prime UTR variant | G/T | snv | 0.11 | 1 | ||
rs10489525 | 1.000 | 0.040 | 1 | 114721064 | intron variant | G/A | snv | 0.32 | 1 | ||
rs1858830 | 0.925 | 0.040 | 7 | 116672385 | 5 prime UTR variant | C/G | snv | 0.40 | 1 | ||
rs4141463 | 0.925 | 0.040 | 20 | 14766825 | intron variant | T/C | snv | 0.50 | 1 | ||
rs7711337 | 1.000 | 0.040 | 5 | 162656512 | intron variant | G/A;C | snv | 1 | |||
rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 1 | |||
rs4675502 | 1.000 | 0.040 | 2 | 205221447 | intron variant | G/A;C | snv | 1 | |||
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 5 |