Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 7
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 7
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs3766606
PARK7
0.827 0.120 1 7962137 intron variant G/T snv 0.22 6
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 6
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 5
rs11581607
IL23R
0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 4
rs12035735
LRRC8D
1 89839786 intron variant G/A snv 1.4E-03 4
rs12103
INTS11 ; PUSL1 ; MIR6727
0.925 0.040 1 1312114 synonymous variant T/A;C;G snv 0.56 3
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 3
rs2488389
DENND1B
0.925 0.040 1 197662011 intron variant G/A snv 0.22 3
rs4656958
ITLN1
0.925 0.040 1 160887174 upstream gene variant A/G;T snv 3
rs6667605
LOC100996583
1.000 0.040 1 2571341 downstream gene variant C/T snv 0.53 3
rs670523
RIT1
1.000 0.040 1 155908941 intron variant A/G snv 0.48 3
rs7554511
INAVA
0.925 0.040 1 200908434 intron variant C/A snv 0.22 3
rs10797432
LOC100996583
1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs10798069
PLA2G4A
1.000 0.040 1 186906327 intron variant G/T snv 0.37 2