Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7554511
INAVA
0.925 0.040 1 200908434 intron variant C/A snv 0.22 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
rs10781499
CARD9
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 2
rs11564258
MUC19 ; LOC105369736
1.000 0.040 12 40398498 intron variant G/A snv 3.1E-02 2
rs11742570 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 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
rs2076756
NOD2
0.882 0.040 16 50722970 intron variant A/G snv 0.17 2
rs2413583 0.925 0.040 22 39263768 intron variant C/T snv 0.19 2
rs3091316 1.000 0.040 17 34266955 upstream gene variant G/A;C snv 2
rs4409764 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 2
rs5743289
NOD2
1.000 0.040 16 50722863 intron variant C/G;T snv 2
rs6568421 1.000 0.040 6 105987150 regulatory region variant A/G snv 0.23 2
rs7927997 1.000 0.040 11 76590331 upstream gene variant C/T snv 0.34 2
rs921720
LOC105375746
1.000 0.040 8 125522429 intron variant A/G snv 0.48 2
rs9822268
APEH
0.925 0.040 3 49682296 intron variant G/A;T snv 2
rs9858542
BSN
0.925 0.040 3 49664550 synonymous variant G/A snv 0.26 0.27 2
rs1000113
IRGM
0.925 0.040 5 150860514 intron variant C/T snv 0.13 1
rs1002922 1.000 0.040 5 40386453 regulatory region variant T/C snv 0.29 1
rs10065637
ANKRD55
1.000 0.040 5 56143024 intron variant C/T snv 0.15 1
rs10117785
TNFSF15
1.000 0.040 9 114789323 3 prime UTR variant T/A snv 0.34 1
rs10181042
PUS10
1.000 0.040 2 60997124 intron variant C/T snv 0.41 1
rs10210302
ATG16L1
1.000 0.040 2 233250193 intron variant C/A;T snv 1
rs1042058
MAP3K8
1.000 0.040 10 30439172 synonymous variant T/C snv 0.51 0.45 1