Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs7775055 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 2
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 2
rs2284033
IL2RB
0.790 0.160 22 37137994 intron variant G/A snv 0.43 2
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18 2
rs12434551 1.000 0.120 14 68786647 downstream gene variant A/C;T snv 1
rs1479924 0.807 0.120 4 122466445 intergenic variant G/A snv 0.76 1
rs2847293 0.807 0.120 18 12782449 downstream gene variant A/G;T snv 1
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10 1
rs7909519
IL2RA
0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02 1
rs4705862
IRF1-AS1
1.000 0.120 5 132477527 intron variant A/T snv 0.51 1
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 1