Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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 1
rs1033180 1.000 0.080 6 383546 regulatory region variant C/T snv 5.4E-02 1
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 2
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 5
rs10883365
LINC01475
0.882 0.080 10 99528007 non coding transcript exon variant G/A snv 0.52 1
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
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 7
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 4
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs11552708
TNFSF12-TNFSF13 ; TNFSF13
0.882 0.240 17 7559238 missense variant G/A;C snv 0.13; 4.2E-06 1
rs11711054 1.000 0.080 3 46304120 intergenic variant G/A snv 0.73 1
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs11734090
KIAA1109
1.000 0.080 4 122306958 intron variant T/C snv 0.25 1
rs11851414
ZFP36L1
1.000 0.080 14 68792785 intron variant T/C snv 0.25 1
rs11875687
PTPN2
1.000 0.080 18 12843138 intron variant T/C snv 0.17 1
rs11938795
KIAA1109
0.882 0.120 4 122151854 upstream gene variant T/C snv 0.24 1
rs12068671 0.925 0.160 1 172711891 intergenic variant T/C snv 0.23 1
rs12142280 1.000 0.080 1 172895512 intron variant T/A snv 0.21 1
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3