Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3917265
IL1R1
1.000 0.120 2 102162001 intron variant T/C snv 0.50 2
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs6419573 1.000 0.120 2 102410643 upstream gene variant T/C snv 0.78 1
rs73510898
ZGLP1
0.925 0.120 19 10305768 intron variant G/A;C;T snv 2
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 2
rs2271404
MIR4435-2HG
1.000 0.120 2 111246290 non coding transcript exon variant T/C snv 0.12 1
rs2041733
CLEC16A ; LOC105371081
1.000 0.120 16 11135732 intron variant T/C;G snv 1
rs12634229 0.882 0.120 3 112657461 intergenic variant T/C snv 0.15 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs6686734
MFN2
1.000 0.120 1 12008884 intron variant T/C snv 0.71 1
rs13132933 0.925 0.200 4 122089432 upstream gene variant T/C snv 0.22 1
rs45616239
KIAA1109
0.925 0.120 4 122335010 intron variant T/C snv 0.13 2
rs17389644 0.925 0.120 4 122576542 intergenic variant G/A;T snv 1
rs9952991 0.925 0.120 18 12780465 upstream gene variant G/A;C snv 2
rs7127307 1.000 0.120 11 128317488 regulatory region variant T/C snv 0.47 1
rs7815944
LINC00824
1.000 0.120 8 128415272 intron variant A/G snv 0.12 1
rs80312298
MGMT
0.925 0.120 10 129683009 intron variant C/A;T snv 2
rs6596086
RAD50
0.925 0.120 5 132616530 intron variant T/C snv 0.34 2
rs6871536
RAD50 ; TH2LCRR
0.827 0.160 5 132634182 intron variant T/C snv 0.24 1
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 2
rs12188917
TH2LCRR ; IL13
1.000 0.120 5 132655393 intron variant T/C;G snv 1
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 3
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4