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
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
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
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
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs10800314 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 5
rs10889676
IL23R
0.827 0.120 1 67256884 intron variant C/A;T snv 5
rs114202211
HIPK1
0.827 0.120 1 113943285 intron variant T/C snv 8.1E-03 5
rs12075255
IL19
0.827 0.120 1 206788283 intron variant A/G snv 0.74 5
rs12131796
INAVA
0.827 0.120 1 200909599 intron variant G/A snv 0.22 5
rs1333062
ITLN1
0.807 0.200 1 160876494 downstream gene variant T/C;G snv 5
rs16841904
DENND1B
0.807 0.160 1 197732862 intron variant C/T snv 0.18 5
rs183686347
IL23R
0.827 0.120 1 67237759 intron variant G/A snv 4.8E-03 5
rs2234161
TNFRSF14
0.827 0.120 1 2559766 non coding transcript exon variant C/T snv 4.1E-05; 0.55 0.58 5
rs3806308
RNF186
0.827 0.120 1 19816373 intron variant C/T snv 0.36 5
rs4655215 0.827 0.120 1 19811221 upstream gene variant T/C snv 0.68 5
rs4971079 0.827 0.120 1 155157915 intergenic variant G/A;C snv 5
rs61802846
FCGR2A
0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 5
rs6425143 0.827 0.120 1 172875212 intron variant T/G snv 0.34 5
rs6600247 0.827 0.120 1 24978623 intergenic variant T/C snv 0.55 5
rs6693105 0.827 0.120 1 152618187 downstream gene variant T/C snv 0.59 5