Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs1260333 | 0.882 | 0.160 | 2 | 27525757 | downstream gene variant | A/G | snv | 0.58 | 12 | ||
rs2911711 | 0.925 | 0.120 | 2 | 27527679 | downstream gene variant | T/A | snv | 0.58 | 6 | ||
rs4666002 | 0.925 | 0.120 | 2 | 27617773 | intron variant | G/A;C | snv | 6 | |||
rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 30 | ||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs4453795 | 3 | 192376186 | intron variant | A/G;T | snv | 2 | |||||
rs10517480 | 4 | 59883111 | intergenic variant | A/T | snv | 0.27 | 2 | ||||
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 13 | ||
rs1000778 | 1.000 | 0.040 | 11 | 61887833 | intron variant | A/G | snv | 0.59 | 3 | ||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 18 | ||
rs108499 | 11 | 61779765 | intron variant | C/T | snv | 0.27 | 2 | ||||
rs1109748 | 11 | 61955173 | synonymous variant | C/A | snv | 0.21 | 0.11 | 2 | |||
rs11230815 | 11 | 61868654 | downstream gene variant | G/C;T | snv | 2 | |||||
rs149803 | 11 | 61771548 | synonymous variant | C/G;T | snv | 0.18 | 2 | ||||
rs1535 | 0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 | 24 | ||
rs17156426 | 11 | 61841851 | intron variant | A/G;T | snv | 2 | |||||
rs17156442 | 11 | 61846551 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs174448 | 1.000 | 0.120 | 11 | 61872101 | downstream gene variant | G/A | snv | 0.61 | 3 | ||
rs174449 | 11 | 61872907 | downstream gene variant | G/A | snv | 0.54 | 2 | ||||
rs174450 | 1.000 | 0.080 | 11 | 61874070 | intron variant | G/T | snv | 0.44 | 3 | ||
rs174455 | 1.000 | 0.080 | 11 | 61888645 | intron variant | G/A;C | snv | 5 | |||
rs174456 | 11 | 61888710 | intron variant | C/A | snv | 0.59 | 2 | ||||
rs174464 | 11 | 61890454 | intron variant | A/G | snv | 0.59 | 2 | ||||
rs174468 | 11 | 61896219 | upstream gene variant | G/A | snv | 0.28 | 2 |