Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs12130219
LOC112268240 ; PUDPP2 ; FLG-AS1
0.925 0.120 1 152189630 non coding transcript exon variant A/G snv 0.23 2
rs1528473 0.925 0.120 15 55094545 downstream gene variant A/G snv 7.6E-02 2
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 2
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 2
rs9357733
EFHC1
0.851 0.160 6 52427338 intron variant A/G snv 0.19 2
rs112111458 0.925 0.120 2 70872975 intergenic variant A/G snv 0.16 1
rs1444418 1.000 0.120 10 62800710 intron variant A/G snv 0.22 1
rs16999165 1.000 0.120 20 54190682 intergenic variant A/G snv 5.5E-02 1
rs176095
PBX2 ; GPSM3
0.925 0.160 6 32190542 upstream gene variant A/G snv 0.22 1
rs7815944
LINC00824
1.000 0.120 8 128415272 intron variant A/G snv 0.12 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs10791824
OVOL1-AS1 ; OVOL1
0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs1665050
RNF111
1.000 0.120 15 59001406 intron variant A/G;T snv 1
rs2918307 1.000 0.120 19 8679458 downstream gene variant A/G;T snv 0.19 1
rs11205006 1.000 0.120 1 152467700 intergenic variant A/T snv 0.72 1
rs77199844
LCE1E
1.000 0.120 1 152784619 upstream gene variant AT/- del 0.12 1
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs1343795
ZNF652
0.882 0.120 17 49334880 intron variant C/A snv 0.78 1