Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10049390 | 0.776 | 0.080 | 3 | 133982275 | intron variant | G/A | snv | 0.67 | 10 | ||
rs1011970 | 0.677 | 0.320 | 9 | 22062135 | intron variant | G/T | snv | 0.23 | 22 | ||
rs1028166 | 0.790 | 0.080 | 4 | 181892145 | intron variant | G/A | snv | 0.74 | 9 | ||
rs10411210 | 0.742 | 0.160 | 19 | 33041394 | intron variant | C/T | snv | 0.22 | 13 | ||
rs10457678 | 0.790 | 0.080 | 6 | 138801103 | intron variant | A/G | snv | 0.19 | 10 | ||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 31 | ||
rs10506868 | 0.716 | 0.160 | 10 | 112559621 | intron variant | C/T | snv | 3.1E-02 | 16 | ||
rs10511330 | 0.776 | 0.080 | 3 | 114402172 | intron variant | T/C | snv | 0.22 | 10 | ||
rs10774214 | 0.790 | 0.080 | 12 | 4259186 | intron variant | T/C | snv | 0.54 | 9 | ||
rs10904849 | 0.790 | 0.080 | 10 | 16955267 | intron variant | G/A;T | snv | 0.25 | 9 | ||
rs10911251 | 0.790 | 0.080 | 1 | 183112059 | intron variant | A/C | snv | 0.37 | 9 | ||
rs10980628 | 0.776 | 0.080 | 9 | 110909123 | intron variant | T/C | snv | 0.16 | 10 | ||
rs11085466 | 0.790 | 0.080 | 19 | 21569009 | intron variant | G/C | snv | 0.23 | 10 | ||
rs11119608 | 0.708 | 0.280 | 1 | 210816167 | intron variant | T/G | snv | 0.21 | 17 | ||
rs11150038 | 0.790 | 0.080 | 16 | 78042662 | intron variant | A/C;G | snv | 10 | |||
rs11168936 | 0.708 | 0.280 | 12 | 49251457 | intron variant | T/A;C | snv | 17 | |||
rs11196170 | 0.776 | 0.080 | 10 | 112962862 | intron variant | G/A;C | snv | 10 | |||
rs11196172 | 0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 | 18 | ||
rs11200014 | 0.695 | 0.280 | 10 | 121575416 | intron variant | G/A;T | snv | 0.34 | 19 | ||
rs113569514 | 0.790 | 0.080 | 3 | 134029945 | intron variant | T/C | snv | 0.23 | 9 | ||
rs114436839 | 0.790 | 0.080 | 3 | 155691561 | intron variant | G/A | snv | 1.8E-03 | 9 | ||
rs115392158 | 0.708 | 0.280 | 6 | 31347004 | intron variant | A/G | snv | 17 | |||
rs11571818 | 0.708 | 0.280 | 13 | 32394673 | intron variant | T/C | snv | 6.6E-03 | 6.0E-03 | 17 | |
rs117079142 | 0.776 | 0.080 | 8 | 116778675 | intron variant | C/A | snv | 3.0E-02 | 10 | ||
rs11844632 | 0.708 | 0.280 | 14 | 68559662 | intron variant | G/A | snv | 0.23 | 17 |