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
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
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
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 2
rs704840
LOC100506023 ; TNFSF4
0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 2
rs1857066
LOC100506023 ; TNFSF4
1.000 0.040 1 173363490 non coding transcript exon variant A/C snv 0.79 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
rs624988 0.925 0.120 1 116721168 regulatory region variant T/A;C snv 1
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 1
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 1
rs924080 0.882 0.240 1 67294457 intergenic variant T/C snv 0.45 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 3
rs3821236
STAT4
0.882 0.160 2 191038032 intron variant G/A snv 0.25 3
rs7601754
STAT4
0.882 0.160 2 191075725 intron variant G/A;T snv 2
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 1
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 1
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 1
rs1372072
PLCL2
0.851 0.200 3 16913767 intron variant G/A snv 0.35 1
rs2176082
PXK
0.925 0.080 3 58345459 intron variant G/A snv 0.36 1
rs35677470
DNASE1L3
0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 1
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 1