Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 3
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 1
rs10220668
LINC01500
1.000 0.040 14 59042487 intron variant A/G snv 0.30 1
rs1035798
AGER
1.000 0.040 6 32183445 splice region variant G/A snv 0.24 0.19 1
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs11047102
SOX5
0.925 0.160 12 23793212 intron variant C/T snv 7.9E-02 1
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 1
rs11171747
ESYT1 ; ZC3H10
1.000 0.040 12 56124624 3 prime UTR variant T/A;G snv 1
rs11191865
STN1
0.925 0.160 10 103913084 intron variant G/A snv 0.44 1
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1133906
SAMD9L
0.925 0.080 7 93135669 synonymous variant C/T snv 0.22 0.28 1
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 1
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 1
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 1
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs11860650
ITGAM
0.882 0.120 16 31315385 intron variant C/T snv 0.14 2
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 1
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10