Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21
rs1130233
AKT1
0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs2075820
NOD1
0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 10
rs6912200
PGC
0.925 0.080 6 41750170 intron variant C/T snv 0.54 3
rs1330344
PTGS1
0.925 0.120 9 122369409 upstream gene variant C/T snv 0.69 2
rs2376549
DEFB121
0.925 0.120 20 31411284 intron variant C/T snv 0.42 2
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs3807987
CAV1
0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs158572
ERCC8 ; NDUFAF2
0.851 0.120 5 60943616 intron variant G/A snv 0.63 4
rs3805246
GAB1
0.882 0.120 4 143382955 intron variant G/A snv 0.31 3
rs1402686368
SERPINE1
1.000 0.040 7 101133793 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1878672
IL19 ; IL10
0.882 0.080 1 206770368 intron variant G/A;C;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
rs7804372
CAV1
0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs2072493
TLR5
0.851 0.280 1 223111257 missense variant T/A;C snv 0.16 4
rs8111085
DNMT1
1.000 0.040 19 10162696 missense variant T/A;C;G snv 1