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
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 1
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 1
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 2
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 1
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 1
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 1
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 2
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 1