Source: GWASDB

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 13
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs2269241
PGM1
1.000 0.120 1 63643100 intron variant T/C snv 0.23 2
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 2
rs12566340
AP4B1-AS1 ; BCL2L15
0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 1
rs672797 1.000 0.120 1 81094869 downstream gene variant C/A;T snv 0.63 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 1
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs11571316
CTLA4
0.925 0.160 2 203866366 upstream gene variant G/A;C snv 1
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 1
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 1
rs478222
EFR3B
1.000 0.120 2 25078886 intron variant A/T snv 0.35 1