Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10065172
IRGM
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 8
rs1018326
LINC01934
1.000 0.080 2 181143073 intron variant T/C snv 0.47 1
rs10188217
PUS10
0.925 0.080 2 60990407 intron variant T/A;C snv 2
rs10203477
LINC01185
0.925 0.200 2 60877850 intron variant A/T snv 0.48 2
rs1033180 1.000 0.080 6 383546 regulatory region variant C/T snv 5.4E-02 1
rs10484718
THEMIS
1.000 0.080 6 127859906 intron variant A/T snv 8.6E-02 1
rs10491434
IL7R
1.000 0.080 5 35877812 3 prime UTR variant A/G snv 0.32 2
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 4
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10796045 1.000 0.080 10 6360779 intergenic variant G/T snv 0.79 1
rs10800746
INAVA
1.000 0.080 1 200912264 intron variant C/T snv 0.32 1
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 6
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs1085308051
PTEN
0.882 0.200 10 87933229 missense variant A/G snv 4.0E-06 6
rs10883365
LINC01475
0.882 0.080 10 99528007 non coding transcript exon variant G/A snv 0.52 3
rs10886159 1.000 0.080 10 117854099 intergenic variant T/C snv 0.25 1
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs10930046
IFIH1
0.882 0.200 2 162281473 missense variant T/C snv 9.7E-02 0.16 3
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 7
rs11100722 1.000 0.080 4 141616307 intergenic variant G/C snv 0.77 1
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14