Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | ||
rs10468017 | 0.851 | 0.120 | 15 | 58386313 | intron variant | C/T | snv | 0.24 | 12 | ||
rs10517480 | 4 | 59883111 | intergenic variant | A/T | snv | 0.27 | 2 | ||||
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 | |||||
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 | ||
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 | ||||
rs174472 | 11 | 61904484 | intron variant | A/G | snv | 0.41 | 2 | ||||
rs174476 | 11 | 61906646 | synonymous variant | C/A;G;T | snv | 0.30 | 2 | ||||
rs174478 | 11 | 61911104 | intron variant | T/G | snv | 0.31 | 2 | ||||
rs174479 | 11 | 61911282 | intron variant | C/G | snv | 0.17 | 2 | ||||
rs174528 | 1.000 | 0.080 | 11 | 61776027 | intron variant | T/C | snv | 0.42 | 0.42 | 5 |