Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 1
rs1005133 1.000 0.120 22 19750832 intergenic variant C/T snv 0.20 1
rs10088748
SGCZ
1.000 0.120 8 14611016 intron variant C/A snv 0.51 1
rs10097964 1.000 0.120 8 21125392 intron variant G/A snv 2.6E-02 1
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 2
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs10175798 1.000 0.120 2 30226728 upstream gene variant G/A snv 0.51 1
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs10203477
LINC01185
0.925 0.200 2 60877850 intron variant A/T snv 0.48 2
rs10209110
AFF3
1.000 0.120 2 100056230 intron variant C/T snv 0.47 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10275421
LNCPRESS1
1.000 0.120 7 101299780 non coding transcript exon variant G/A snv 7.2E-02 1
rs1042663
C2 ; CYP21A2 ; C2-AS1
0.925 0.160 6 31937353 synonymous variant G/A snv 9.7E-02 0.12 1
rs1043099
CASTOR1
1.000 0.120 22 30285268 3 prime UTR variant C/A;G;T snv 1
rs1046080
PRRC2A
1.000 0.120 6 31628105 missense variant C/A snv 0.79 0.74 1
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 2
rs10484565
TAP2
0.925 0.200 6 32827255 3 prime UTR variant G/A snv 6.1E-02 1
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 2
rs1049281
HLA-C
1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 2
rs10494360
FCGR2A
1.000 0.120 1 161505960 non coding transcript exon variant G/A snv 0.10 9.0E-02 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 1
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 1
rs10520789 1.000 0.120 15 95598638 regulatory region variant G/A snv 0.12 1