Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1487309678 | 0.851 | 0.280 | 7 | 84014246 | missense variant | C/T | snv | 8.0E-06 | 5 | ||
rs739439 | 0.851 | 0.200 | 17 | 28396803 | 3 prime UTR variant | C/T | snv | 0.13 | 5 | ||
rs11466285 | 0.851 | 0.200 | 2 | 70450307 | 3 prime UTR variant | A/C;G | snv | 5 | |||
rs3771523 | 0.851 | 0.200 | 2 | 70450336 | 3 prime UTR variant | C/T | snv | 0.14 | 5 | ||
rs1269636220 | 0.851 | 0.280 | 10 | 120865109 | missense variant | A/G | snv | 5 | |||
rs12543318 | 0.882 | 0.120 | 8 | 87856112 | intergenic variant | C/A | snv | 0.68 | 4 | ||
rs572007403 | 0.882 | 0.200 | 19 | 919955 | missense variant | C/A | snv | 3.3E-04 | 9.1E-05 | 4 | |
rs4791774 | 0.882 | 0.240 | 17 | 9028802 | intron variant | A/C;G | snv | 4 | |||
rs4791331 | 0.925 | 0.120 | 17 | 9028765 | intron variant | C/T | snv | 0.53 | 3 | ||
rs7043516 | 1.000 | 0.080 | 9 | 97855151 | 3 prime UTR variant | A/C;T | snv | 2 | |||
rs3775261 | 1.000 | 0.080 | 4 | 4862018 | intron variant | C/A | snv | 0.30 | 2 | ||
rs3821949 | 1.000 | 0.080 | 4 | 4858675 | upstream gene variant | G/A | snv | 0.32 | 2 |