Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs61747728
NPHS2
0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs33388
NR3C1
0.776 0.360 5 143317730 intron variant A/T snv 0.53 12
rs1071630
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
0.851 0.120 6 32641349 missense variant T/A;C snv 0.49 4
rs33389
NR3C1
0.882 0.280 5 143320934 intron variant C/G;T snv 4
rs1129740
HLA-DQA2 ; LOC107986589 ; HLA-DQA1
0.882 0.080 6 32641328 missense variant G/A snv 0.49 0.26 3
rs1136759
HLA-DRB1
0.882 0.080 6 32584354 missense variant C/A;G;T snv 8.9E-03; 0.23; 1.2E-04 3
rs17878703
HLA-DRB1
0.882 0.080 6 32584360 missense variant G/A;C;T snv 2.6E-02; 5.7E-04; 0.18; 1.3E-05 3
rs1063348
HLA-DQB1-AS1 ; HLA-DQB1
1.000 0.080 6 32660146 3 prime UTR variant A/G snv 0.43 2
rs1140343
HLA-DQB1
1.000 0.080 6 32661360 missense variant T/C;G snv 0.20 0.50 1