Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs1384936174
NOD2
0.827 0.040 16 50710812 missense variant G/A;T snv 4.0E-06; 4.0E-06 6
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 6
rs2076756
NOD2
0.882 0.040 16 50722970 intron variant A/G snv 0.17 5
rs3735656
MAFK
1.000 0.040 7 1541285 3 prime UTR variant C/G;T snv 5
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 4
rs10226620
TMEM184A ; MAFK
1.000 0.040 7 1541881 3 prime UTR variant T/C snv 0.69 4
rs11581607
IL23R
0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 4
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 4
rs2066843
NOD2
0.925 0.040 16 50711288 synonymous variant C/A;T snv 0.19 4
rs272879
MIR3936HG ; SLC22A4
0.882 0.040 5 132334853 synonymous variant C/A;G;T snv 4.0E-06; 0.57 4
rs3814055
NR1I2
0.925 0.040 3 119781188 5 prime UTR variant C/T snv 0.35 4
rs3814057
NR1I2
0.925 0.040 3 119818407 3 prime UTR variant A/C snv 0.28 4
rs7240004 1.000 0.040 18 48868651 intergenic variant A/G snv 0.43 4
rs7720838 0.925 0.040 5 40486794 intron variant G/T snv 0.52 4
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs962917
MYO9B
0.882 0.040 19 17191438 intron variant G/A snv 0.45 4
rs1049526
BRD2
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93 3
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3
rs10781499
CARD9
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 3
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 3
rs11064881
CIT
1.000 0.040 12 119709120 intron variant G/A snv 5.0E-02 3
rs113653754
HLA-DQB1-AS1
0.925 0.040 6 32658495 upstream gene variant C/A snv 3
rs11641184
LITAF
0.925 0.040 16 11610795 intron variant C/A snv 0.36 3
rs11741861
ZNF300 ; IRGM
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02 3