Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs10808546 8 125483576 intron variant C/T snv 0.39 7