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
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
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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 3
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs2153977
MAGI3
0.807 0.240 1 113537449 intron variant C/T snv 0.28 2
rs2358994
BCL2L15 ; AP4B1-AS1
0.925 0.120 1 113886839 intron variant G/A snv 0.16 2
rs559047 1.000 0.120 1 238590616 intergenic variant T/A;C snv 2
rs2269241
PGM1
1.000 0.120 1 63643100 intron variant T/C snv 0.23 1
rs6691977
CAMSAP2
1.000 0.120 1 200845831 intron variant T/C snv 0.32 1
rs7533564
MGC27382 ; PTGFR
0.925 0.120 1 78360228 intron variant C/T snv 0.92 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14