Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 3
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 3
rs3828309
ATG16L1
0.882 0.160 2 233271764 intron variant A/G snv 0.42 3
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 3
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv 3
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 3
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs7554511
INAVA
0.925 0.040 1 200908434 intron variant C/A snv 0.22 3
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 3
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18 3
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 3
rs10495903
THADA
1.000 0.040 2 43579779 intron variant C/T snv 0.13 2
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 2
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 2
rs11564258
MUC19 ; LOC105369736
1.000 0.040 12 40398498 intron variant G/A snv 3.1E-02 2
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 2
rs1250546
ZMIZ1
0.925 0.080 10 79272775 intron variant A/G snv 0.36 2
rs12722489
IL2RA
0.882 0.160 10 6060049 intron variant C/T snv 0.11 2
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs151181
CLN3
1.000 0.040 16 28479196 intron variant T/C snv 0.32 2
rs2062305
LINC02341
1.000 0.040 13 42478744 intron variant G/A snv 0.46 2
rs2071538
TAP1 ; PSMB9
0.925 0.160 6 32850901 intron variant G/A snv 0.18 0.17 2