Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12757998 0.925 0.080 1 182569343 downstream gene variant C/T snv 0.24 3
rs554219 0.925 0.080 11 69516874 regulatory region variant C/A;G;T snv 3
rs7309332 1.000 0.040 12 7938243 upstream gene variant T/C snv 0.59 3
rs2155222 11 76642761 intergenic variant G/A;T snv 2
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 2
rs7040869 1.000 0.080 9 99072866 downstream gene variant G/A snv 0.11 2
rs7187167 1.000 0.040 16 1299208 upstream gene variant T/C snv 0.69 2
rs10788160 10 121274035 intergenic variant G/A snv 0.19 1
rs10878640 12 67643308 intergenic variant G/T snv 0.32 1
rs12827748 12 79694798 intron variant T/C snv 0.50 1
rs2155225 11 76640853 intergenic variant A/T snv 0.61 1
rs6082527 20 2256129 intron variant G/A snv 0.88 1
rs62355902 1.000 0.080 5 56757896 intergenic variant A/T snv 0.15 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
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs201661522
ABCB1
1.000 0.080 7 87539293 missense variant A/G snv 6.4E-05 1.0E-04 2
rs765189442
ABCB11
0.925 0.080 2 168995422 missense variant T/C snv 8.1E-06 4
rs200246711
ABCB6
2 219216057 missense variant C/A;T snv 2.0E-04 1
rs35628
ABCC1
1.000 0.080 16 16077249 intron variant A/G snv 0.13 1
rs17822931
ABCC11
0.827 0.080 16 48224287 missense variant C/G;T snv 4.0E-06; 0.22 0.13 7
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs2273697
ABCC2
0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 11
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs17268122
ABCC4
1.000 0.080 13 95192240 intron variant G/A;C;T snv 2