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
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs10791824
OVOL1-AS1 ; OVOL1
0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 3
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 3
rs380743
RASIP1
0.925 0.120 19 48737757 intron variant G/A;C snv 2
rs4705962
KIF3A
0.925 0.160 5 132693166 3 prime UTR variant T/A;C snv 2
rs62176107
PRKRA ; CHROMR
0.925 0.120 2 178436244 missense variant G/A;T snv 2
rs73510898
ZGLP1
0.925 0.120 19 10305768 intron variant G/A;C;T snv 2
rs80312298
MGMT
0.925 0.120 10 129683009 intron variant C/A;T snv 2
rs9952991 0.925 0.120 18 12780465 upstream gene variant G/A;C snv 2
rs10738626 1.000 0.120 9 22373458 intergenic variant C/G;T snv 1
rs10888499 1.000 0.120 1 152560266 intergenic variant C/A;T snv 1
rs12144049 1.000 0.120 1 152468434 intergenic variant C/G;T snv 1
rs12188917
TH2LCRR ; IL13
1.000 0.120 5 132655393 intron variant T/C;G snv 1
rs148203517
HLA-B ; MIR6891
1.000 0.120 6 31356323 missense variant G/A;T snv 1
rs1665050
RNF111
1.000 0.120 15 59001406 intron variant A/G;T snv 1
rs17389644 0.925 0.120 4 122576542 intergenic variant G/A;T snv 1
rs2041733
CLEC16A ; LOC105371081
1.000 0.120 16 11135732 intron variant T/C;G snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs2592555
PRR5L
1.000 0.120 11 36350207 intron variant T/C;G snv 1
rs2897442
KIF3A
0.925 0.120 5 132713335 intron variant C/A;T snv 1
rs4809219
RTEL1 ; RTEL1-TNFRSF6B
1.000 0.120 20 63671762 intron variant C/A;G;T snv 1