Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs761357
LINC00271
0.851 0.040 6 135581461 intron variant A/G;T snv 5
rs10444776
LOC112268138
0.882 14 105647030 upstream gene variant G/A;T snv 4
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv 4
rs142647938
KCNH7
0.882 2 162516642 intron variant C/A;T snv 4
rs1800601
NTRK1 ; SH2D2A
0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 4
rs1921445 0.882 3 106229671 intergenic variant A/C;G snv 4
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 4
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4
rs4077515
CARD9
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 4
rs67927699
PUS10
0.882 2 60960280 intron variant G/C;T snv 4
rs7005834
CCN4
0.827 0.160 8 133201961 intron variant C/A;T snv 4
rs773107
RAB5B
0.882 12 55975722 intron variant A/G;T snv 4
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 4
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 3
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 3
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 3
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 3
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 2
rs1772408
IFI16
1 159035859 intron variant A/G;T snv 2