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
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
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
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
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
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 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