Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74817271
TNIP1
0.807 0.120 5 151090412 intron variant G/A snv 5.0E-02 6
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 6
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13 2
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 1
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 1
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 1
rs6062496
TNFRSF6B ; RTEL1-TNFRSF6B
0.827 0.120 20 63697746 intron variant G/A snv 0.52 6
rs1860545
TNFRSF1A
0.790 0.200 12 6337611 intron variant G/A snv 0.31 5
rs2234161
TNFRSF14
0.827 0.120 1 2559766 non coding transcript exon variant C/T snv 4.1E-05; 0.55 0.58 5
rs582757
TNFAIP3
0.776 0.320 6 137876687 intron variant C/T snv 0.70 5
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 1
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 2
rs77981966
THADA
0.827 0.120 2 43550825 intron variant C/T snv 4.6E-02 5
rs11691685
TEX41
0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02 5
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs72977586
STK11
0.827 0.120 19 1186317 intron variant G/C snv 0.16 5
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 3