Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1891320 0.925 0.080 1 19970618 upstream gene variant C/T snv 0.20 2
rs1915087
CD86
0.925 0.080 3 122119944 3 prime UTR variant T/C snv 2
rs2027432
NLRP3
0.882 0.160 1 247415139 upstream gene variant A/G;T snv 3
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs2069948
PROCR ; MMP24-AS1-EDEM2
0.851 0.160 20 35174686 non coding transcript exon variant C/T snv 0.55 0.62 5
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 8
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2232618
LBP
0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12 5
rs2234237
TREM1
0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 9
rs2234246
TREM1
0.827 0.240 6 41276002 3 prime UTR variant C/T snv 0.44 5
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6