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
rs11714843
TIMMDC1
0.807 0.120 3 119502217 intron variant T/A snv 0.15 6
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
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
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
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs6894249
IRF1-AS1
0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45 9
rs6946509 0.807 0.120 7 22769871 downstream gene variant T/A;C snv 6
rs7069750
FAS
0.807 0.120 10 89002619 non coding transcript exon variant G/C;T snv 0.50 6
rs7127214
PRR5L
0.807 0.120 11 36322143 intron variant C/G;T snv 6
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs72698115
IL6R ; IL6R-AS1
0.807 0.120 1 154406893 intron variant A/C snv 7.2E-02 6