Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9989163 14 102768675 downstream gene variant G/A snv 0.45 1
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 3
rs9911533 1.000 0.080 17 40619224 intergenic variant C/T snv 0.67 2
rs9901146 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 2
rs9889262
ZNF652
17 49320708 intron variant T/A snv 0.28 3
rs9864529
LPP
1.000 0.040 3 188387268 intron variant G/A snv 0.52 1
rs9860547
LPP
0.925 0.080 3 188411191 intron variant G/A snv 0.34 3
rs9851967
LPP
1.000 0.040 3 188369840 intron variant C/T snv 0.35 1
rs9775039 0.925 0.120 9 6177453 intergenic variant G/A snv 0.20 3
rs9739070 12 123286485 upstream gene variant A/G snv 0.75 1
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 5
rs962993 10 9011169 regulatory region variant C/T snv 0.34 1
rs9573092
KLF5
13 73053137 upstream gene variant A/G;T snv 0.32 1
rs950881
IL18R1 ; IL1RL1
1.000 0.120 2 102316052 intron variant G/A;T snv 2
rs9397706
IPCEF1
6 154341513 intron variant A/G snv 0.52 1
rs9383820
ARID1B
6 157098374 intron variant C/G;T snv 1
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs9323612 14 75502265 intergenic variant A/G snv 0.35 1
rs9303280
GSDMB
1.000 0.080 17 39917778 non coding transcript exon variant T/A;C snv 1
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 3
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 3
rs9273374
HLA-DQB1-AS1
1.000 0.080 6 32658837 upstream gene variant A/G;T snv 2
rs9266772 6 31384336 upstream gene variant T/C snv 0.18 1
rs9259819
HLA-A ; HCG4B
6 29925798 upstream gene variant G/T snv 0.49 1
rs921650
GSDMB
1.000 0.080 17 39912823 intron variant G/A snv 0.60 1