Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs696
NFKBIA
0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 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
rs748113
VSIR ; CDH23
10 71749034 3 prime UTR variant T/C snv 0.38 3
rs149290349
ZFP36L2
2 43224818 missense variant G/A;T snv 6.7E-02 3
rs1822534 3 12225304 intergenic variant A/G;T snv 2
rs58106596 2 231714669 downstream gene variant G/A;C snv 2
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs34664882
ANK1
8 41686157 missense variant G/A snv 2.3E-02 2.1E-02 2
rs62111672
ARHGEF18
19 7350159 intron variant G/A snv 2.6E-02 2
rs713909
CBX7
22 39136415 non coding transcript exon variant G/A;C;T snv 2
rs7578575
DNMT3A
2 25265950 intron variant T/A snv 0.27 2
rs10411936
EPS15L1
1.000 0.080 19 16437564 intron variant A/G snv 0.63 2
rs3131643
HCP5
6 31475005 intron variant G/A snv 0.12 2
rs2249742
HLA-B ; HLA-C
0.925 0.120 6 31272944 intron variant C/T snv 0.50 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs3540
IQGAP1
15 90502176 3 prime UTR variant G/A snv 0.43 2
rs2522056
IRF1-AS1
5 132466034 intron variant G/A snv 0.25 2
rs2347784
KDELR2
7 6485212 upstream gene variant C/G snv 0.29 2
rs552599526
KLF3
4 38675391 intron variant C/-;CC;CCC;CCCC;CCCCC;CCCCCC delins 2
rs2229094
LOC100287329 ; LTA
0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 2