Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs719250
IL1R2
0.827 0.200 2 102007256 intron variant C/T snv 0.11 5
rs3218896
IL1R2
0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs3218977
IL1R2
0.807 0.240 2 102024739 3 prime UTR variant A/G snv 0.14 6
rs10490571
IL1R1
0.827 0.320 2 102100877 intron variant C/T snv 0.29 5
rs1520220
LINC02456 ; IGF1
0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs2195239
LINC02456 ; IGF1
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28 7
rs2033562 1.000 0.120 8 102535511 intron variant G/A;C;T snv 1
rs17019602
VAV3
1.000 0.120 1 107646236 intron variant A/G snv 0.19 1
rs10488764
FDX1
1.000 0.120 11 110460907 intron variant G/A snv 0.18 1
rs4849121
ACOXL
0.925 0.160 2 110842129 intron variant G/A snv 0.44 3
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs11102930
NGF-AS1 ; NGF
0.925 0.160 1 115338434 intron variant G/A snv 0.54 2
rs7389
TREH ; PHLDB1
1.000 0.120 11 118657756 3 prime UTR variant T/G snv 0.32 1
rs13124532
LOC645513 ; PDE5A
1.000 0.120 4 119495290 3 prime UTR variant C/T snv 0.10 2
rs4077515
CARD9
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 11
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1369270 1.000 0.120 2 153179546 intron variant T/C snv 1
rs11264793
FCRL3
1.000 0.120 1 157677736 3 prime UTR variant A/T snv 0.28 1
rs11264794
FCRL3
1.000 0.120 1 157677999 3 prime UTR variant C/A snv 0.63 2
rs6691569
FCRL3
1.000 0.120 1 157678308 3 prime UTR variant G/A snv 0.24 1
rs7522061
FCRL3
0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51 4
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6