Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs506027
ATG5
0.925 0.080 6 106326589 upstream gene variant G/A snv 0.57 2
rs5744105
TLR5
0.925 0.080 1 223142735 intron variant G/C snv 0.57 2
rs595209
TIRAP
0.925 0.080 11 126292326 intron variant A/C;G snv 2
rs8177375
TIRAP
0.925 0.080 11 126293169 3 prime UTR variant A/G snv 0.12 0.13 2
rs117983287
VPS13A
1.000 0.080 9 77405958 missense variant C/A snv 9.6E-03 8.3E-03 1
rs150062338
LPP
1.000 0.080 3 188287160 intron variant C/T snv 3.6E-02 1
rs58764888
HRH1
1.000 0.080 3 11176005 intron variant T/A snv 5.8E-02 1
rs945177
LOC105370124
1.000 0.080 13 27047848 intergenic variant G/A;T snv 1
rs9529561 1.000 0.080 13 69325374 downstream gene variant A/G snv 6.3E-02 1
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15
rs2857656
CCL2
0.851 0.120 17 34254988 upstream gene variant G/A;C snv 5
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs368287711
IL10RA
0.851 0.120 11 117989554 missense variant C/A;T snv 2.0E-05; 2.4E-05 4
rs11137480
S1PR3 ; C9orf47
0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs17036188
PPARG
0.882 0.120 3 12299426 intron variant T/C snv 4.0E-02 3
rs2664581
PI3
0.882 0.120 20 45175881 missense variant A/C snv 0.16 0.16 3
rs2839693
CXCL12
0.882 0.120 10 44379119 intron variant T/A;C snv 3
rs374520012
LBP
0.882 0.120 20 38373994 missense variant T/C;G snv 8.0E-06; 4.0E-06 3
rs5743867
TOLLIP
0.882 0.120 11 1307121 intron variant G/A;C snv 3
rs7022797
C9orf47 ; S1PR3
0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3
rs7119750
RELA
0.882 0.120 11 65655120 3 prime UTR variant C/G;T snv 3
rs773520745
IL12RB1
0.882 0.120 19 18075817 missense variant C/G;T snv 2.0E-05; 4.0E-06 3
rs805305
DDAH2
0.882 0.120 6 31729610 intron variant C/G snv 0.48 3
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7