Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234711
IFNGR1
0.827 0.080 6 137219383 5 prime UTR variant A/G snv 0.43 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs7608910
PUS10
0.827 0.120 2 60977721 intron variant A/G snv 0.37 6
rs104895467
NOD2
0.851 0.120 16 50716899 missense variant A/G snv 1.2E-03 7.5E-04 5
rs2076756
NOD2
0.882 0.040 16 50722970 intron variant A/G snv 0.17 5
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 4
rs4795397
ZPBP2
0.925 0.160 17 39867492 upstream gene variant A/G snv 0.38 4
rs7240004 1.000 0.040 18 48868651 intergenic variant A/G snv 0.43 4
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3
rs11741861
ZNF300 ; IRGM
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02 3
rs1250546
ZMIZ1
0.925 0.080 10 79272775 intron variant A/G snv 0.36 3
rs35873774
XBP1
0.925 0.040 22 28795944 intron variant A/G snv 4.6E-02 3
rs376377228
C1orf141 ; IL23R
0.925 0.040 1 67182950 missense variant A/G snv 1.6E-05 2.1E-05 3
rs449454
NDFIP1
0.925 0.080 5 142153497 3 prime UTR variant A/G snv 0.65 0.68 3
rs670523
RIT1
1.000 0.040 1 155908941 intron variant A/G snv 0.48 3
rs6962966
MAGI2
0.925 0.120 7 78174806 intron variant A/G snv 0.50 3
rs758102857
C1orf141 ; IL23R
0.925 0.040 1 67206957 missense variant A/G snv 4.0E-06 3
rs7657746
KIAA1109
0.925 0.040 4 122240464 intron variant A/G snv 0.24 3
rs7796976
LOC101927609 ; AHR
0.925 0.040 7 17298806 5 prime UTR variant A/G snv 0.79 3
rs10491434
IL7R
1.000 0.080 5 35877812 3 prime UTR variant A/G snv 0.32 2
rs11548656
PLCG2
1.000 0.040 16 81883307 missense variant A/G snv 2.5E-02 2.7E-02 2
rs1238539471
NOD2
1.000 0.040 16 50710637 synonymous variant A/G snv 7.0E-06 2
rs12627970 1.000 0.080 22 39325740 TF binding site variant A/G snv 0.19 2
rs1292053
TUBD1
1.000 0.040 17 59886176 missense variant A/G snv 0.45 0.46 2