Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs10056340 0.925 0.080 5 110854353 intergenic variant T/G snv 0.31 2
rs1007654
GSDMA
1.000 0.080 17 39955101 intron variant A/G snv 0.69 1
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs10173081
IL1RL1 ; IL18R1
1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs10174949
LINC00299
1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23 1
rs10178845
LINC00299
1.000 0.080 2 8303673 intron variant G/A snv 0.23 1
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs10192157
IL18R1 ; IL1RL1
1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 2
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs10204137
IL18R1 ; IL1RL1
0.925 0.160 2 102351752 missense variant A/G;T snv 0.34 1
rs10206753
IL18R1 ; IL1RL1
1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 2
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 1
rs10211025 1.000 0.080 2 41801493 intergenic variant A/G snv 0.12 1
rs1039559
TLR6 ; TLR1
1.000 0.080 4 38829975 intron variant G/A snv 0.62 1
rs1043828
WDR36
1.000 0.080 5 111128310 3 prime UTR variant T/C;G snv 2
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 1
rs10508372 1.000 0.080 10 8930055 intergenic variant G/A snv 0.14 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs1054609
ZPBP2
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 2
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 1
rs1059288
RGL2 ; TAPBP
0.882 0.320 6 33299895 3 prime UTR variant A/G snv 0.60 1
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 1