Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs1130233
AKT1
0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs1550117
DNMT3A
0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs2075820
NOD1
0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 10
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43 6
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 5
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs158572
ERCC8 ; NDUFAF2
0.851 0.120 5 60943616 intron variant G/A snv 0.63 4
rs718226
LOC102724907
0.882 0.120 16 50735652 intron variant A/G snv 0.36 4
rs2709800
NOD1
0.882 0.120 7 30473155 intron variant A/C snv 0.53 4
rs2301756
PTPN11
0.851 0.120 12 112452972 intron variant A/G snv 0.21 4
rs2072493
TLR5
0.851 0.280 1 223111257 missense variant T/A;C snv 0.16 4
rs3805246
GAB1
0.882 0.120 4 143382955 intron variant G/A snv 0.31 3
rs1878672
IL19 ; IL10
0.882 0.080 1 206770368 intron variant G/A;C;T snv 3
rs2015620
IL32
0.882 0.120 16 3073560 intron variant A/G;T snv 3
rs6912200
PGC
0.925 0.080 6 41750170 intron variant C/T snv 0.54 3
rs1640827
TLR5
0.882 0.120 1 223138265 intron variant C/G;T snv 3
rs17163737
TLR5
0.882 0.120 1 223129809 intron variant G/T snv 7.2E-02 3
rs2243086
CHRNE ; GP1BA
1.000 0.040 17 4930914 intron variant G/T snv 0.20 2
rs6490061
CUX2
0.925 0.120 12 111335541 intron variant T/C snv 0.30 2
rs2376549
DEFB121
0.925 0.120 20 31411284 intron variant C/T snv 0.42 2