Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs10781499
CARD9
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 3
rs4077515
CARD9
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 4
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs501916
SEMA6D
1.000 0.040 15 47761032 synonymous variant C/A snv 0.40 0.41 2
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 4
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 2
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 2
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs707939
MSH5-SAPCD1 ; MSH5
0.851 0.200 6 31758911 intron variant C/A snv 0.34 0.26 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs12718244
SPATA48
0.827 0.120 7 50136058 intron variant G/A snv 0.33 0.33 6
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 6
rs2236379
PRKCQ
0.790 0.160 10 6485181 missense variant G/A snv 0.31 0.30 6
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 1
rs181206
IL27
0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24 2
rs3764147
LACC1
0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 3
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 3
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 3
rs9858542
BSN
0.925 0.040 3 49664550 synonymous variant G/A snv 0.26 0.27 2
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 7