Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs6584283
LINC01475
0.776 0.080 10 99530544 intron variant T/C snv 0.56 12
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 11
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
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
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 8
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46 5
rs6993442 8 129683891 upstream gene variant G/C snv 0.17 5
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 5
rs11327184
CCDC26
8 129592027 intron variant C/- delins 0.40 4
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 4