Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 | ||
rs1801260 | 0.695 | 0.280 | 4 | 55435202 | 3 prime UTR variant | A/G | snv | 0.25 | 28 | ||
rs746284240 | 0.763 | 0.240 | 12 | 68809243 | missense variant | A/G | snv | 11 | |||
rs934945 | 0.827 | 0.200 | 2 | 238246412 | missense variant | C/T | snv | 0.21 | 0.15 | 10 | |
rs7602358 | 0.827 | 0.080 | 2 | 238147187 | intron variant | G/T | snv | 0.83 | 6 | ||
rs3027178 | 0.882 | 0.040 | 17 | 8149767 | synonymous variant | T/G | snv | 0.30 | 0.29 | 3 |