Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44 6
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46 5
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18 5
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 5
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs13092376
PAK2
3 196789417 intron variant A/C;G snv 0.33 3
rs62237617
TTC28
22 28365160 intron variant C/G;T snv 1.9E-03 3
rs79716587
ARHGAP15
2 143129250 intron variant G/A snv 7.9E-02 3
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 3
rs10087240
PVT1
8 128000328 intron variant C/G;T snv 2
rs10411936
EPS15L1
1.000 0.080 19 16437564 intron variant A/G snv 0.63 2
rs1285886
RREB1
6 7140598 intron variant G/A snv 0.28 2
rs17041439
SPIC
12 101479462 intron variant A/C snv 7.0E-02 2
rs1883932
LOC105372521 ; PLCB1
20 8628941 intron variant A/T snv 0.58 2
rs2249742
HLA-B ; HLA-C
0.925 0.120 6 31272944 intron variant C/T snv 0.50 2
rs2284344
TNFRSF1A
12 6336163 intron variant G/C snv 0.49 2
rs247826
MEAK7
16 84549359 intron variant C/T snv 0.18 2
rs2522056
IRF1-AS1
5 132466034 intron variant G/A snv 0.25 2
rs3131643
HCP5
6 31475005 intron variant G/A snv 0.12 2