Source: GWASCAT ×
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 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
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 3
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 2
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
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 1
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 1
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 15
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 3
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
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs11217040 0.925 0.200 11 118809939 regulatory region variant C/A snv 0.19 2
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11552708
TNFSF12-TNFSF13 ; TNFSF13
0.882 0.240 17 7559238 missense variant G/A;C snv 0.13; 4.2E-06 1
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 1
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14