Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 6
rs9366778
LINC02571 ; LOC112267902 ; HLA-B
0.925 0.120 6 31301396 intron variant G/A snv 0.47 6
rs9391858
TSBP1-AS1 ; TSBP1
0.925 0.080 6 32373621 intron variant A/G snv 0.13 6
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12 5
rs1894406
HLA-DOB
0.925 0.120 6 32819279 intron variant C/G;T snv 5
rs2071472
HLA-DOB
0.925 0.120 6 32816843 intron variant C/T snv 0.34 0.27 5
rs2071474
HLA-DOB
0.925 0.120 6 32814805 intron variant C/T snv 0.27 5
rs2249742
HLA-B ; HLA-C
0.925 0.120 6 31272944 intron variant C/T snv 0.50 5
rs2256175
MICA
1.000 6 31412672 intron variant C/T snv 0.55 5
rs2395471
HLA-B ; HLA-C
0.925 0.120 6 31272915 intron variant G/A snv 0.47 5
rs241440
TAP2
0.925 0.120 6 32829584 intron variant C/G;T snv 0.30 5
rs2523619
HLA-B
0.925 0.120 6 31350367 intron variant T/C snv 0.23 5
rs2524123
HLA-B ; LINC02571 ; LOC112267902
0.925 0.040 6 31297537 intron variant T/C snv 0.34 5
rs2534678
MICB ; MICB-DT
0.925 0.120 6 31496186 intron variant G/A;T snv 5
rs2736171
PRRC2A
0.925 0.120 6 31627710 intron variant A/G snv 0.34 5
rs2844472
PRRC2A ; SNORA38
0.925 0.120 6 31621899 intron variant A/G snv 0.29 5
rs2844615
HLA-B
1.000 6 31275182 intron variant C/T snv 0.11 5
rs2844795
TRIM31 ; TRIM31-AS1
0.925 0.120 6 30106070 intron variant C/G;T snv 5
rs2857106
HLA-DOB
0.925 0.120 6 32819793 intron variant T/C snv 0.19 5
rs2905722
MICB-DT
0.925 0.120 6 31481550 intron variant A/G snv 0.88 5
rs3130558
PSORS1C1
0.925 0.080 6 31129406 intron variant C/G snv 0.77 5
rs3131009
PSORS1C1
0.925 0.080 6 31131055 intron variant G/A;C snv 5
rs3131034
DDR1
0.925 0.080 6 30886019 intron variant G/A snv 0.75 5
rs34214527
TNXB
0.925 0.040 6 32046679 intron variant C/T snv 0.11 5
rs3871466
MUC22
0.925 0.120 6 31015906 intron variant T/C snv 0.12 5