Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 6
rs10483639 1.000 0.040 14 54839739 downstream gene variant G/C snv 0.26 3
rs17197936 0.925 0.040 13 37601702 upstream gene variant T/C snv 5.2E-02 3
rs13093031 1.000 0.120 3 88809891 intergenic variant A/G snv 0.17 2
rs13361160 1.000 0.040 5 10169711 downstream gene variant T/C snv 0.34 2
rs1972597 1.000 0.040 17 77598082 intron variant T/C snv 0.31 2
rs3862188 1.000 0.040 1 247702471 intron variant T/C snv 0.44 2
rs6961071 1.000 0.120 7 156182007 downstream gene variant A/G;T snv 0.47 2
rs943552 1 156885826 downstream gene variant C/T snv 9.7E-02 2
rs12633508 3 88765985 intergenic variant T/C snv 0.23 1
rs1571138 1 46429969 upstream gene variant A/G snv 0.73 1
rs17122021 11 118274971 regulatory region variant C/A;T snv 1
rs17289394 13 46899085 upstream gene variant G/A snv 0.33 1
rs2383515 1 186683820 upstream gene variant G/A;T snv 1
rs398655 13 33013514 upstream gene variant A/C snv 0.51 1
rs4660928 1 46420268 TF binding site variant A/C snv 0.63 1
rs7335912 13 95015426 upstream gene variant A/G snv 0.16 1
rs73633565 X 13459192 intergenic variant A/G snv 0.14 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2756109
ABCC2
10 99798989 intron variant G/T snv 0.53 1
rs9524885
ABCC4
13 95283335 intron variant T/C snv 0.63 2
rs4584690
ABCC4
13 95027878 intron variant T/C;G snv 1
rs4512126
ABLIM3
5 149166179 intron variant T/A;C snv 1
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 17