Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131665
IRF7
0.851 0.160 11 613208 missense variant T/C snv 0.25 0.33 4
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1149386 1.000 0.120 1 160471451 TF binding site variant G/C snv 0.96 1
rs11571297 0.882 0.120 2 203880280 regulatory region variant T/C snv 0.44 3
rs11571302 0.925 0.200 2 203878211 downstream gene variant G/A;T snv 2
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs11652878
ITGAE
0.925 0.160 17 3751686 missense variant A/C;G snv 4.0E-06; 0.12 2
rs1167204443
GAD1
0.882 0.160 2 170829475 missense variant G/C snv 4.0E-06 1.4E-05 3
rs11675434
TPO
0.827 0.240 2 1404043 non coding transcript exon variant C/T snv 0.39 5
rs116869525 0.925 0.160 6 32421366 intergenic variant C/T snv 3.5E-03 2
rs12050151
CEP128
1.000 0.120 14 80902473 intron variant T/C;G snv 1
rs1207011218
CTLA4
0.742 0.440 2 203870794 synonymous variant C/T snv 12
rs12101255
TSHR
0.925 0.120 14 80984708 intron variant C/T snv 0.37 2
rs12101261
TSHR
1.000 0.120 14 80984885 intron variant C/T snv 0.37 1
rs12136280
LINC01136
1.000 0.120 1 203302802 intron variant G/T snv 0.35 1
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24 9
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908864
TSHR ; LOC101928462
0.851 0.120 14 81143416 missense variant T/C;G snv 4.0E-06 6
rs121908873
TSHR ; LOC101928462
0.790 0.160 14 81139828 missense variant G/A;T snv 7
rs1230666
MAGI3
0.925 0.200 1 113630788 intron variant A/G snv 0.90 2
rs12451295 0.925 0.280 17 70380682 intergenic variant C/T snv 0.61 2
rs12526548
FGFR1OP
1.000 0.120 6 167017659 intron variant C/T snv 0.43 1
rs12653715
JAKMIP2 ; LOC105378218
1.000 0.120 5 147732794 intron variant G/C snv 0.13 1
rs1265883
SLAMF6
1.000 0.120 1 160495121 intron variant C/A;G snv 0.96 1