Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs867114783 | 17 | 7675109 | missense variant | T/C | snv | 5 | |||||
rs7668666 | 1.000 | 4 | 186080138 | intron variant | C/A;T | snv | 4 | ||||
rs11121704 | 1 | 11233902 | intron variant | C/A;T | snv | 3 | |||||
rs2660852 | 12 | 96051770 | intergenic variant | C/A | snv | 0.34 | 3 | ||||
rs1156560901 | 2 | 201880120 | missense variant | A/G | snv | 1.4E-05 | 2 | ||||
rs1212415280 | 6 | 43771130 | missense variant | G/T | snv | 2.1E-05 | 2 | ||||
rs1308088661 | 17 | 39727880 | missense variant | G/A | snv | 4.0E-06 | 2 | ||||
rs181264737 | 8 | 124589710 | missense variant | C/A;G;T | snv | 1.2E-05; 4.1E-06; 4.1E-06 | 2 | ||||
rs723526 | 1.000 | 7 | 55067126 | intron variant | A/G | snv | 0.86 | 2 | |||
rs753066745 | X | 81277164 | missense variant | C/T | snv | 1.7E-05 | 9.5E-06 | 2 | |||
rs771308693 | 8 | 140752306 | missense variant | G/A | snv | 3.2E-05 | 7.0E-06 | 2 | |||
rs1053129 | 5 | 80626901 | 3 prime UTR variant | C/A;T | snv | 1 | |||||
rs10964859 | 9 | 21140673 | 3 prime UTR variant | C/A;G | snv | 1 | |||||
rs10964862 | 9 | 21151554 | intergenic variant | C/A;G | snv | 1 | |||||
rs1317052311 | X | 15358134 | missense variant | C/A | snv | 5.5E-06 | 1 | ||||
rs1472189 | 11 | 11962338 | 3 prime UTR variant | C/T | snv | 0.25 | 1 | ||||
rs148626207 | 4 | 102612593 | missense variant | T/C | snv | 8.0E-06 | 1.4E-05 | 1 | |||
rs200246209 | 11 | 102527789 | synonymous variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |||
rs2375801 | 4 | 186550471 | intron variant | T/C | snv | 0.34 | 1 | ||||
rs2994809 | 1 | 119809354 | intron variant | T/C | snv | 0.91 | 1 | ||||
rs3206652 | 3 | 108046402 | 3 prime UTR variant | T/C | snv | 0.27 | 1 | ||||
rs370006648 | 15 | 23687168 | missense variant | G/A | snv | 4.1E-05 | 7.0E-05 | 1 | |||
rs377767422 | 10 | 43119635 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 | |||
rs3804639 | 3 | 108071988 | intron variant | G/T | snv | 0.28 | 1 | ||||
rs684559 | 1 | 111215824 | intron variant | G/A | snv | 0.27 | 1 |