Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs3754093
EXO1
0.776 0.240 1 241846814 upstream gene variant A/G snv 0.23 11
rs636832
AGO1
0.790 0.400 1 35897874 intron variant G/A snv 0.23 8
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs2070150
ATF6
0.827 0.280 1 161791486 missense variant G/C snv 0.14 9.2E-02 6
rs11465817
IL23R
0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs4649203 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 4
rs4656942
CD244
0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs485618
CD244
0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54 4
rs7536540
MIR101-1 ; MIR3671 ; JAK1
0.882 0.160 1 65058899 intron variant C/G;T snv 0.65 3
rs7549785
FCER1A
0.925 0.080 1 159308078 3 prime UTR variant G/A snv 0.13 3
rs10918706
CD247
0.925 0.200 1 167496884 intron variant C/T snv 0.24 2
rs12133337
CD247
0.925 0.160 1 167483453 intron variant T/C snv 0.17 2
rs1329044438
DIO1
0.925 0.120 1 53906244 missense variant G/A snv 2
rs17127024
JAK1
0.925 0.280 1 64837448 intron variant G/T snv 5.1E-02 2
rs10912564
TNFSF4
1.000 0.080 1 173201479 intron variant C/T snv 0.43 1
rs4244165
JAK1
1.000 0.080 1 64955388 intron variant G/C;T snv 1
rs7525481
IFNLR1
1.000 0.080 1 24154900 3 prime UTR variant C/T snv 0.54 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92