Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 8
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 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
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 7
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs2081687 0.882 0.240 8 58476006 intergenic variant T/C snv 0.70 6
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 5
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 5