Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 4
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 2
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 2
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 2
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 1
rs2647045 6 32700323 TF binding site variant G/A snv 0.27 1
rs4530903 6 32614112 intergenic variant C/T snv 0.10 1
rs751837
CDC42BPB
0.882 0.120 14 103018488 intron variant T/C snv 0.23 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs707824
LOC101928354
0.925 0.120 6 14636732 intergenic variant T/C snv 0.74 1
rs6773854
LOC105374265
1.000 0.120 3 187931631 downstream gene variant T/C snv 0.23 1
rs12289961
OR10Q2P
11 58292720 non coding transcript exon variant C/T snv 0.28 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 1
rs948562
ZFP91-CNTF ; ZFP91
11 58580292 intron variant A/G snv 0.15 1