Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
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
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 4
rs10791824
OVOL1-AS1 ; OVOL1
0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 3
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 3
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 2
rs12081541 0.925 0.160 1 152468890 intergenic variant T/C snv 8.9E-02 2
rs12130219
LOC112268240 ; PUDPP2 ; FLG-AS1
0.925 0.120 1 152189630 non coding transcript exon variant A/G snv 0.23 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
rs1384974 0.925 0.120 3 177009491 downstream gene variant T/C snv 9.6E-02 2
rs1528473 0.925 0.120 15 55094545 downstream gene variant A/G snv 7.6E-02 2
rs167769
STAT6
0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 2
rs17690965
KIF3A
0.925 0.160 5 132694975 3 prime UTR variant C/G snv 0.57 2
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 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
rs2251396
MICA-AS1
0.827 0.240 6 31396930 upstream gene variant G/A snv 0.24 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