Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs1058026
HLA-B
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21 5
rs13211318 0.925 0.040 6 32134903 upstream gene variant A/C snv 0.11 5
rs7751505 1.000 6 31392478 downstream gene variant A/C snv 0.31 5
rs28367646
LINC02571 ; LOC112267902 ; HLA-B
1.000 6 31300555 intron variant A/C snv 0.36 4
rs38152
LOC101927668
1.000 7 20007952 intron variant A/C snv 6.2E-02 4
rs9468914
HLA-B
1.000 6 31282829 intron variant A/C snv 0.40 4
rs3131018
POU5F1 ; PSORS1C3
1.000 6 31175805 intron variant A/C;G snv 4
rs3130424 0.925 0.040 6 31250462 intergenic variant A/C;G;T snv 5
rs3130779 0.925 0.080 6 30904426 upstream gene variant A/C;G;T snv 5
rs10456057
HLA-B ; USP8P1
1.000 6 31277757 non coding transcript exon variant A/C;G;T snv 0.13 4
rs28481932
HLA-B
1.000 6 31275123 intron variant A/C;G;T snv 0.20 4
rs3778639
PSORS1C1
1.000 6 31125999 intron variant A/C;G;T snv 4
rs3755319
UGT1A8 ; UGT1A1 ; UGT1A3 ; UGT1A4 ; UGT1A7 ; UGT1A10 ; UGT1A9 ; UGT1A5 ; UGT1A6
0.925 0.120 2 233758936 intron variant A/C;G;T snv 3
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29 6
rs2844509
SNORD84 ; DDX39B-AS1 ; DDX39B ; ATP6V1G2-DDX39B
0.882 0.160 6 31543147 intron variant A/G snv 0.23 6
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6
rs6906846
HLA-B ; USP8P1
0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 6
rs9391858
TSBP1-AS1 ; TSBP1
0.925 0.080 6 32373621 intron variant A/G snv 0.13 6
rs241448
TAP2
0.882 0.200 6 32828908 stop lost A/G snv 0.32 0.27 5
rs2523674
HCP5
0.925 0.120 6 31469012 non coding transcript exon variant A/G snv 0.54 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
rs2905722
MICB-DT
0.925 0.120 6 31481550 intron variant A/G snv 0.88 5