Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9297145
KPNA7
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67 1
rs1870293
SETD1A
0.827 0.120 16 30959620 intron variant T/C snv 0.62 1
rs27524
ERAP1 ; CAST
0.851 0.160 5 96766240 intron variant A/G snv 0.61 1
rs4649203 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 1
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 1
rs8016947 0.925 0.080 14 35363460 intron variant T/G snv 0.60 1
rs2700987
ELMO1
1.000 0.040 7 37346633 intron variant C/A snv 0.60 1
rs892085
QTRT1
0.925 0.040 19 10707416 intron variant G/A snv 0.57 0.59 1
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 2
rs7404095
PRKCB
0.827 0.120 16 23853269 intron variant T/C snv 0.58 1
rs610604
TNFAIP3
0.827 0.240 6 137878280 intron variant G/T snv 0.58 2
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 3
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 1
rs10782001
FBXL19
1.000 0.040 16 30931304 intron variant G/A snv 0.53 2
rs4676406 0.827 0.120 2 240639691 intergenic variant G/T snv 0.53 1
rs2546890
LOC285626
0.882 0.200 5 159332892 non coding transcript exon variant A/G snv 0.52 2
rs13708
STX1B ; HSD3B7
1.000 0.040 16 30989488 3 prime UTR variant G/A;C snv 0.52 1
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 1
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 1
rs7849191
JAK2
0.882 0.120 9 4988761 intron variant C/T snv 0.50 1
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 2
rs3762999
TNIP1
1.000 0.040 5 151089865 intron variant C/T snv 0.49 1
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 1
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2