Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6809854
LOC105376976
1.000 0.040 3 18742931 intron variant A/G snv 0.19 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 1
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 1
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 3
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 2
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 2
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2
rs2082412 0.925 0.120 5 159290781 downstream gene variant G/A snv 0.27 2
rs2546890
LOC285626
0.882 0.200 5 159332892 non coding transcript exon variant A/G snv 0.52 2
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 2
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs1473247
RNF145
1.000 0.040 5 159176563 intron variant T/C snv 0.41 1
rs151823
ERAP1
1.000 0.040 5 96824289 intron variant A/C snv 0.90 1
rs2233278
TNIP1
0.925 0.040 5 151087628 5 prime UTR variant G/C;T snv 4.8E-02 1
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 1
rs27524
ERAP1 ; CAST
0.851 0.160 5 96766240 intron variant A/G snv 0.61 1
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs3213094
IL12B ; LOC107986469
0.925 0.080 5 159323761 intron variant C/G;T snv 0.26 1
rs3762999
TNIP1
1.000 0.040 5 151089865 intron variant C/T snv 0.49 1
rs6863411
NDFIP1
0.827 0.120 5 142133639 intron variant A/T snv 0.67 1