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
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 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
rs6475611 9 22151140 intergenic variant G/A snv 0.21 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
rs11171739
ERBB3
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 4
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs3812049
SLC12A2 ; LINC01184
5 128083158 non coding transcript exon variant C/A;G;T snv 4
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs13092376
PAK2
3 196789417 intron variant A/C;G snv 0.33 3
rs28577594
RILPL2
12 123411359 3 prime UTR variant G/C snv 0.56 3
rs61387190
SMG9
19 43756777 upstream gene variant C/A;T snv 3
rs62237617
TTC28
22 28365160 intron variant C/G;T snv 1.9E-03 3
rs696
NFKBIA
0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 3
rs748113
VSIR ; CDH23
10 71749034 3 prime UTR variant T/C snv 0.38 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
rs9494142
LOC105378010
6 135110502 TF binding site variant T/C snv 0.21 3