Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 11
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 8
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7