Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs367569
LOC105371082 ; RMI2
0.807 0.120 16 11271643 intron variant C/T snv 0.32 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs114202211
HIPK1
0.827 0.120 1 113943285 intron variant T/C snv 8.1E-03 5
rs661054
NXPE1 ; NXPE2
0.827 0.120 11 114559688 intron variant A/G;T snv 5
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 1
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 6
rs7468800 0.827 0.120 9 114829725 regulatory region variant C/A snv 0.11 5
rs726657
DELEC1
0.827 0.120 9 114934056 intron variant C/T snv 0.50 6
rs7195296 0.827 0.120 16 11655918 intergenic variant A/C;G snv 5
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 1
rs72977586
STK11
0.827 0.120 19 1186317 intron variant G/C snv 0.16 5
rs4319543 1.000 0.040 12 122160501 intergenic variant A/C snv 0.35 1
rs11059675
LRRC43
1.000 0.040 12 122183779 intron variant G/A snv 0.43 1
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 1
rs45616239
KIAA1109
0.925 0.120 4 122335010 intron variant T/C snv 0.13 2
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs59867199 0.827 0.120 4 122531076 intergenic variant C/G;T snv 5
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 6
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs6697886 0.827 0.120 1 1238231 downstream gene variant G/A snv 0.21 5