Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 11 | ||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 10 | ||
rs7138803 | 0.827 | 0.240 | 12 | 49853685 | intergenic variant | G/A;T | snv | 6 | |||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 5 | ||
rs10913469 | 1.000 | 0.080 | 1 | 177944384 | intron variant | T/C | snv | 0.22 | 5 | ||
rs633715 | 1.000 | 0.080 | 1 | 177883445 | intron variant | T/C | snv | 0.17 | 4 | ||
rs6548238 | 0.882 | 0.200 | 2 | 634905 | TF binding site variant | T/C | snv | 0.85 | 4 | ||
rs1558902 | 0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 | 4 | ||
rs2815752 | 0.925 | 0.200 | 1 | 72346757 | intron variant | G/A | snv | 0.62 | 4 | ||
rs314277 | 0.925 | 0.080 | 6 | 104959787 | intron variant | A/C;G;T | snv | 3 | |||
rs5742915 | 0.925 | 0.080 | 15 | 74044292 | missense variant | T/C;G | snv | 0.35; 4.0E-06 | 3 | ||
rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 3 | ||
rs1659127 | 16 | 14294448 | intergenic variant | G/A;C;T | snv | 2 | |||||
rs4549631 | 6 | 126645162 | intron variant | T/C;G | snv | 2 | |||||
rs543874 | 1.000 | 0.080 | 1 | 177920345 | upstream gene variant | A/G | snv | 0.21 | 2 | ||
rs7846385 | 8 | 77247943 | intergenic variant | T/C | snv | 0.23 | 2 | ||||
rs314268 | 6 | 104970103 | intron variant | G/A | snv | 0.64 | 2 | ||||
rs7759938 | 0.925 | 0.120 | 6 | 104931079 | intron variant | C/T | snv | 0.62 | 2 | ||
rs9391253 | 6 | 104919741 | intron variant | A/T | snv | 0.29 | 2 | ||||
rs7861820 | 9 | 106174393 | intron variant | T/C | snv | 0.62 | 2 | ||||
rs3101336 | 1.000 | 0.080 | 1 | 72285502 | intron variant | T/C | snv | 0.62 | 2 | ||
rs12374521 | 5 | 148457317 | intron variant | C/T | snv | 0.45 | 2 | ||||
rs3810291 | 19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 | 2 | ||||
rs1079866 | 0.925 | 0.080 | 7 | 41430495 | intergenic variant | C/G | snv | 0.13 | 1 | ||
rs10940138 | 5 | 67898641 | intron variant | C/T | snv | 0.21 | 1 |