Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11666254
FPR2 ; FPR1
0.925 0.080 19 51759909 intron variant A/G snv 0.28 2
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs414171
MAPKAPK3 ; CISH
0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
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
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv 5
rs77874543
TNFRSF13C
0.882 0.080 22 41926712 missense variant G/C;T snv 6.1E-02 5.5E-02 3
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
rs17446614
FOXO1
0.851 0.240 13 40565740 intron variant G/A snv 0.16 5
rs2721068
FOXO1
0.882 0.160 13 40565575 intron variant T/C snv 0.38 4
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs374520012
LBP
0.882 0.120 20 38373994 missense variant T/C;G snv 8.0E-06; 4.0E-06 3
rs2232618
LBP
0.851 0.160 20 38373117 missense variant T/C snv 9.2E-02 0.12 5
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs4755453
TRAF6 ; RAG1
0.925 0.080 11 36509094 intron variant C/A;G;T snv 2
rs12605436
MIR187
0.925 0.080 18 35906684 upstream gene variant C/T snv 9.1E-02 2
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 15