Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72920202
JAK1
0.882 1 64895266 intron variant A/T snv 0.15 4
rs72743477
SMAD3
0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs7100025
ANKRD30A ; LINC00993
0.724 0.240 10 37303610 intron variant G/A snv 0.68 14
rs7088058
PLEKHA1
0.851 0.040 10 122389836 intron variant C/T snv 0.32 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs7005834
CCN4
0.827 0.160 8 133201961 intron variant C/A;T snv 4
rs6914622
SASH1
0.851 0.040 6 148193165 regulatory region variant G/T snv 0.33 5
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 4
rs67927699
PUS10
0.882 2 60960280 intron variant G/C;T snv 4
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs5865
TMEM131
0.851 0.040 2 97756543 3 prime UTR variant C/T snv 0.62 5
rs57791671 0.882 3 121889586 upstream gene variant T/A snv 0.38 4
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18 5
rs56817615
CLNK
0.882 4 10717222 intergenic variant A/G snv 0.42 4
rs55984493 0.851 0.040 13 99118074 intergenic variant A/T snv 0.15 5
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs4761587
PLXNC1
0.882 12 94158023 intron variant A/G snv 0.78 4