Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8061882
CLEC16A
0.827 0.120 16 11067551 intron variant G/C snv 0.11 5
rs11065898
SH2B3
1.000 0.040 12 111424771 intron variant C/T snv 0.21 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs11649613
LOC107984859
0.827 0.120 16 11225500 downstream gene variant C/T snv 0.37 5
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 6
rs367569
LOC105371082 ; RMI2
0.807 0.120 16 11271643 intron variant C/T snv 0.32 6
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
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
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 1
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
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
rs72977586
STK11
0.827 0.120 19 1186317 intron variant G/C snv 0.16 5
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