Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1002481 | 0.882 | 0.080 | 6 | 111390819 | intron variant | T/A;G | snv | 3 | |||
rs10040363 | 0.882 | 0.080 | 5 | 83177826 | intron variant | A/G | snv | 0.50 | 3 | ||
rs10053847 | 0.882 | 0.080 | 5 | 35878038 | 3 prime UTR variant | G/A | snv | 0.13 | 3 | ||
rs10054203 | 0.882 | 0.080 | 5 | 1279849 | intron variant | G/A;C;T | snv | 3 | |||
rs1014264982 | 0.882 | 0.080 | 19 | 3577038 | missense variant | G/A;C | snv | 6.8E-06 | 7.0E-06 | 3 | |
rs10187911 | 0.882 | 0.080 | 2 | 50420809 | intron variant | C/A;G;T | snv | 3 | |||
rs10244817 | 0.882 | 0.080 | 7 | 124827416 | intron variant | T/C | snv | 0.22 | 3 | ||
rs10412613 | 0.882 | 0.080 | 19 | 52209575 | intron variant | G/A | snv | 0.63 | 3 | ||
rs1043973338 | 0.882 | 0.080 | 2 | 112830483 | missense variant | A/C | snv | 3 | |||
rs10487372 | 0.882 | 0.080 | 7 | 117560845 | intron variant | C/T | snv | 0.13 | 3 | ||
rs1049337 | 0.882 | 0.080 | 7 | 116560533 | 3 prime UTR variant | C/T | snv | 0.25 | 3 | ||
rs10508266 | 0.882 | 0.080 | 10 | 3797822 | intergenic variant | G/A;T | snv | 3 | |||
rs10512948 | 0.882 | 0.080 | 5 | 8233238 | intron variant | T/C | snv | 0.15 | 3 | ||
rs10519203 | 0.851 | 0.080 | 15 | 78521704 | intron variant | G/A | snv | 0.67 | 3 | ||
rs1052486 | 0.851 | 0.200 | 6 | 31642909 | missense variant | A/G | snv | 0.51 | 0.44 | 3 | |
rs1053566 | 0.882 | 0.080 | 19 | 7911079 | missense variant | C/T | snv | 3 | |||
rs1057519857 | 0.882 | 0.080 | 17 | 39724772 | missense variant | T/C | snv | 3 | |||
rs1057519984 | 0.882 | 0.080 | 17 | 7673777 | missense variant | G/C;T | snv | 3 | |||
rs1060503291 | 0.882 | 0.080 | 5 | 112835135 | missense variant | C/T | snv | 3 | |||
rs1062980 | 0.827 | 0.080 | 15 | 78500185 | 3 prime UTR variant | T/C | snv | 0.39 | 3 | ||
rs10750417 | 0.882 | 0.080 | 11 | 129612280 | non coding transcript exon variant | A/G;T | snv | 3 | |||
rs10853100 | 0.882 | 0.080 | 17 | 48525070 | downstream gene variant | T/C | snv | 0.41 | 3 | ||
rs11020802 | 0.882 | 0.080 | 11 | 94493959 | upstream gene variant | C/A;G;T | snv | 3 | |||
rs11072768 | 0.882 | 0.080 | 15 | 78637136 | intron variant | T/C;G | snv | 3 | |||
rs11090910 | 0.882 | 0.080 | 22 | 46111790 | non coding transcript exon variant | T/C | snv | 0.30 | 3 |