Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 9
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
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs9942416 5 75741470 intergenic variant C/G snv 0.53 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
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 8
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 8
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7