Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 3
rs704840
LOC100506023 ; TNFSF4
0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 2
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 1
rs3131917 0.882 0.080 5 173230018 upstream gene variant T/G snv 0.52 1
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 1
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 1
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs2523477 0.925 0.080 6 31392612 downstream gene variant T/C snv 0.10 3
rs9275390 0.882 0.120 6 32701379 downstream gene variant T/C snv 0.30 3
rs1635852
JAZF1
0.882 0.160 7 28149792 intron variant T/C snv 0.42 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 2
rs4963128
PHRF1
0.882 0.120 11 589564 intron variant T/C snv 0.64 2
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 1
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 1
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs2275247
KIAA0319L
0.925 0.080 1 35442850 intron variant T/C snv 0.26 1
rs3790566
IL12RB2
1.000 0.040 1 67348757 intron variant T/C snv 0.61 1
rs924080 0.882 0.240 1 67294457 intergenic variant T/C snv 0.45 1
rs11171747
ESYT1 ; ZC3H10
1.000 0.040 12 56124624 3 prime UTR variant T/A;G snv 1
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4