Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs7759127
HLA-B ; HLA-C
0.925 0.040 6 31273211 intron variant T/G snv 0.11 5
rs3764147
LACC1
0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs4574921 0.882 0.160 9 114776054 upstream gene variant C/T snv 0.80 2
rs3753395
CFH
0.882 0.120 1 196717522 intron variant A/G;T snv 2
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 2
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13 2
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs2853930
WASF5P ; HLA-B
1.000 0.040 6 31287647 non coding transcript exon variant A/C;T snv 0.10 2
rs10982385 1.000 0.040 9 114730737 intergenic variant T/G snv 0.47 1
rs1587601 1.000 0.040 5 35254508 intergenic variant A/G snv 0.64 1
rs16948876 1.000 0.040 16 50820507 intergenic variant G/A snv 6.2E-02 1
rs2844573 0.882 0.160 6 31367677 intron variant A/C;G snv 1
rs28490179 1.000 0.040 6 32551228 upstream gene variant C/T snv 0.81 1
rs40457 1.000 0.040 8 89811459 intergenic variant A/G snv 0.58 1
rs7194886 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 1
rs9271348 0.925 0.160 6 32615965 regulatory region variant G/A snv 0.74 1
rs9302752 0.925 0.120 16 50685192 upstream gene variant T/C snv 0.68 1
rs3762318
C1orf141
0.925 0.040 1 67131436 intron variant G/A snv 0.83 1
rs3088362
CCDC122
1.000 0.040 13 43859494 intron variant C/A;T snv 1
rs9533634
CCDC122
1.000 0.040 13 43823679 downstream gene variant T/C snv 0.53 1
rs2951916
FILIP1 ; UBE2V1P15
1.000 0.040 6 75465141 non coding transcript exon variant A/G snv 0.51 1
rs9270856
HLA-DRB1
1.000 0.040 6 32603062 intergenic variant A/G snv 0.74 1
rs9271100
HLA-DRB1
0.925 0.120 6 32608701 regulatory region variant T/A;C snv 1