Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11086102 | 0.882 | 19 | 18287818 | upstream gene variant | G/C | snv | 0.64 | 6 | |||
rs6475611 | 9 | 22151140 | intergenic variant | G/A | snv | 0.21 | 6 | ||||
rs13063578 | 3 | 47046347 | intron variant | T/A | snv | 0.46 | 5 | ||||
rs6993442 | 8 | 129683891 | upstream gene variant | G/C | snv | 0.17 | 5 | ||||
rs913678 | 0.882 | 0.240 | 20 | 50338887 | regulatory region variant | T/C | snv | 0.51 | 5 | ||
rs11327184 | 8 | 129592027 | intron variant | C/- | delins | 0.40 | 4 | ||||
rs12711490 | 0.925 | 0.080 | 16 | 85939422 | intron variant | T/C | snv | 0.18 | 4 | ||
rs13138355 | 4 | 82624823 | upstream gene variant | C/A;T | snv | 4 | |||||
rs13277237 | 8 | 129592317 | intron variant | G/A | snv | 0.53 | 4 | ||||
rs1700159 | 1.000 | 0.040 | 12 | 51912002 | intron variant | C/A;G;T | snv | 4 | |||
rs2239630 | 0.925 | 0.160 | 14 | 23120140 | upstream gene variant | A/C;G | snv | 4 | |||
rs413141 | 19 | 6675978 | downstream gene variant | A/G | snv | 0.84 | 4 | ||||
rs4432538 | 20 | 8626746 | intron variant | G/A | snv | 0.52 | 4 | ||||
rs45577137 | 8 | 47739071 | upstream gene variant | A/G;T | snv | 4 | |||||
rs72699818 | 14 | 92611266 | intron variant | T/C | snv | 0.12 | 4 | ||||
rs7288670 | 22 | 24225858 | intron variant | A/C;G | snv | 4 | |||||
rs9880192 | 1.000 | 0.040 | 3 | 128578726 | upstream gene variant | G/A;C | snv | 0.31 | 4 | ||
rs10418046 | 19 | 53824615 | upstream gene variant | T/G | snv | 0.26 | 3 | ||||
rs10980797 | 9 | 111150273 | intron variant | A/G;T | snv | 3 | |||||
rs11190141 | 1.000 | 0.040 | 10 | 99532633 | upstream gene variant | C/T | snv | 0.40 | 3 | ||
rs113760175 | 6 | 22343363 | intron variant | G/A;T | snv | 3 | |||||
rs1157008 | 9 | 88920798 | regulatory region variant | T/C;G | snv | 3 | |||||
rs11611647 | 12 | 4224753 | intergenic variant | T/C | snv | 0.22 | 3 | ||||
rs11642657 | 16 | 85982722 | intron variant | C/A;T | snv | 3 | |||||
rs117758012 | 1.000 | 0.080 | 19 | 12846836 | intron variant | C/T | snv | 4.1E-02 | 3 |