Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 7
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 6
rs35667974
IFIH1
0.776 0.280 2 162268127 missense variant T/C snv 1.1E-02 1.2E-02 6
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 6
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 6
rs4976646
RGS14
0.851 0.200 5 177361569 intron variant T/C snv 0.41 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 5
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 5
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 5
rs3747517
IFIH1
0.732 0.360 2 162272314 missense variant T/C snv 0.68 0.68 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 5
rs10797431
LOC100996583
0.851 0.080 1 2569783 non coding transcript exon variant G/T snv 0.42 5