Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 2
rs2412973
HORMAD2
1.000 0.080 22 30133642 intron variant C/A snv 0.54 2
rs2413583 0.925 0.040 22 39263768 intron variant C/T snv 0.19 2
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 2
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 2
rs5743289
NOD2
1.000 0.040 16 50722863 intron variant C/G;T snv 2
rs6871626 0.851 0.160 5 159399784 intron variant C/A;G snv 0.29 2
rs7134599
IFNG-AS1 ; LOC107984526
1.000 0.040 12 68106295 intron variant G/A snv 0.32 2
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs7608910
PUS10
0.827 0.120 2 60977721 intron variant A/G snv 0.37 2
rs8049439
ATXN2L
0.925 0.120 16 28826194 intron variant T/C;G snv 0.38 2
rs921720
LOC105375746
1.000 0.040 8 125522429 intron variant A/G snv 0.48 2
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 2
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 1
rs10065637
ANKRD55
1.000 0.040 5 56143024 intron variant C/T snv 0.15 1
rs10486483
SKAP2
1.000 0.040 7 26852821 intron variant G/A snv 0.21 1
rs10521318 16 85977731 intron variant C/G;T snv 1
rs10896794
LPXN
11 58571651 intron variant T/C snv 0.19 1
rs11612508
DUSP16
12 12504579 intron variant A/G snv 0.22 1
rs11741861
ZNF300 ; IRGM
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02 1
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 1
rs11879191
CDC37
1.000 0.040 19 10402235 intron variant G/A;C snv 1
rs12199775
PHACTR2
6 143577757 intron variant A/G snv 4.8E-02 1
rs12521868
IRF1-AS1
1.000 0.040 5 132448701 intron variant G/T snv 0.28 1
rs12722515
IL2RA
1.000 0.040 10 6039267 intron variant C/A snv 0.13 1