Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 2
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 2
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 2
rs2059876
CHST8
0.925 0.120 19 33639430 intron variant C/T snv 0.28 2
rs2533291
PTPRN2
0.925 0.120 7 157712962 intron variant C/T snv 0.12 2
rs2944542
ZNF365
0.925 0.120 10 62610240 intron variant C/G snv 0.71 2
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 2
rs380743
RASIP1
0.925 0.120 19 48737757 intron variant G/A;C snv 2
rs3917265
IL1R1
1.000 0.120 2 102162001 intron variant T/C snv 0.50 2
rs45616239
KIAA1109
0.925 0.120 4 122335010 intron variant T/C snv 0.13 2
rs6548123
MYT1L
0.925 0.120 2 2221629 intron variant C/T snv 0.76 2
rs6596086
RAD50
0.925 0.120 5 132616530 intron variant T/C snv 0.34 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
rs9357733
EFHC1
0.851 0.160 6 52427338 intron variant A/G snv 0.19 2
rs10199605
LINC00299
1.000 0.120 2 8354967 intron variant G/A snv 0.26 1
rs10995251
LOC105378327 ; ZNF365
1.000 0.120 10 62638706 intron variant C/T snv 0.29 1
rs12188917
TH2LCRR ; IL13
1.000 0.120 5 132655393 intron variant T/C;G snv 1
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 1
rs1343795
ZNF652
0.882 0.120 17 49334880 intron variant C/A snv 0.78 1
rs1444418 1.000 0.120 10 62800710 intron variant A/G snv 0.22 1