Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38 2
rs9889262
ZNF652
17 49320708 intron variant T/A snv 0.28 3
rs2893907
ZNF365
10 62622599 intron variant A/C snv 0.65 1
rs2766678
ZNF217
20 53591817 intron variant G/A snv 0.86 1
rs61977073
TTC6
1.000 0.120 14 37682050 intron variant A/G snv 0.16 2
rs111914382
TTC6
14 37627796 intron variant -/G delins 0.20 1
rs1998359
TTC6
14 37607943 intron variant C/G;T snv 1
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 2
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 2
rs3806932
TSLP
0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 1
rs3806933
TSLP
0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 1
rs4574025
TNFRSF11A
0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs5029937
TNFAIP3
0.882 0.160 6 137874014 intron variant G/T snv 0.13 2
rs148906978
TLR1 ; TLR6
1.000 0.080 4 38852748 intron variant C/T snv 0.29 2
rs28393318
TLR10
1.000 0.080 4 38782646 intron variant A/G snv 0.29 2
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 3
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 2
rs11727978
TLR1
4 38809430 intron variant T/A snv 0.14 1
rs2101521
TLR1
0.925 0.080 4 38809930 intron variant G/A;T snv 1
rs4543123
TLR1
0.882 0.080 4 38790903 non coding transcript exon variant A/G snv 0.32 1
rs6815814
TLR1
1.000 0.080 4 38814717 intron variant A/C snv 0.43 1
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 3
rs3091307
TH2LCRR
0.925 0.160 5 132653444 intron variant A/G snv 0.34 2
rs201333164
SUFU
10 102518505 intron variant GTCT/-;GTCTGTCT;GTCTGTCTGTCT delins 6.7E-04 1