Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs10194635
LINC01104
0.807 0.120 2 100217755 intron variant T/A;G snv 6
rs10213692
ANKRD55
0.807 0.120 5 56146422 intron variant T/C snv 0.17 6
rs10849448
LTBR
0.807 0.120 12 6384185 5 prime UTR variant A/G snv 0.82 6
rs11074967
LOC105371082 ; LOC400499 ; RMI2
0.807 0.120 16 11377557 intron variant C/G snv 0.36 6
rs114940806
KLF17
0.882 0.120 1 44093000 intron variant A/G snv 5.4E-02 3
rs11714843
TIMMDC1
0.807 0.120 3 119502217 intron variant T/A snv 0.15 6
rs1178121
HDAC9
0.882 0.120 7 18723029 intron variant C/A snv 0.31 3
rs12517545
LINC01331
0.882 0.120 5 74384489 intron variant G/A snv 0.13 3
rs1279094 0.882 0.120 9 11706771 intron variant T/C snv 0.43 3
rs1479924 0.807 0.120 4 122466445 intergenic variant G/A snv 0.76 6
rs149850873
PTPN2
0.807 0.120 18 12885121 intron variant G/A snv 1.7E-02 6
rs1823549 0.882 0.120 1 102682275 intergenic variant T/C snv 0.89 3
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18 8
rs2284033
IL2RB
0.790 0.160 22 37137994 intron variant G/A snv 0.43 7
rs2476491
IL2RA
0.776 0.240 10 6053447 intron variant A/T snv 0.25 6
rs27293
LNPEP
0.807 0.120 5 97021474 intron variant A/G;T snv 6
rs2847293 0.807 0.120 18 12782449 downstream gene variant A/G;T snv 6
rs34132030
LINC02341
0.807 0.120 13 42481900 intron variant C/T snv 0.26 6
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs3825568
ZFP36L1
0.807 0.120 14 68793871 5 prime UTR variant C/G;T snv 6
rs41291794 0.882 0.120 6 32457985 downstream gene variant A/T snv 7.5E-02 3
rs45539732
STAT1
0.807 0.120 2 191009521 intron variant T/C snv 1.9E-02 6
rs4648881 0.807 0.120 1 24870664 intergenic variant G/A snv 0.47 6
rs481331 0.882 0.120 10 42507600 intergenic variant A/T snv 0.80 3