Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10760187 0.925 0.040 9 121803541 intergenic variant T/A;C snv 2
rs13145041 0.925 0.040 4 189616909 intergenic variant A/C;G;T snv 2
rs6815464
MAEA
0.925 0.120 4 1316113 intron variant C/G;T snv 2
rs7086701 0.925 0.040 10 10298081 intergenic variant G/A;T snv 2
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs1397780760
LOC105371777 ; KRT20
0.925 0.160 17 40884835 stop gained G/T snv 7.0E-06 2
rs17879146
BIRC5
0.925 0.040 17 78223864 3 prime UTR variant T/G snv 1.2E-02 1.2E-02 2
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs13237474 0.925 0.040 7 135816721 intron variant C/T snv 2.3E-02 2
rs2227532
CXCL8
0.882 0.120 4 73739815 upstream gene variant T/C snv 2.9E-02 3
rs9979250
LOC400867
0.925 0.040 21 38911809 intron variant C/T snv 3.1E-02 2
rs2229092
LTA ; LOC100287329
1.000 0.040 6 31572980 missense variant A/C snv 4.7E-02 4.2E-02 1
rs77490164
NKAIN2
0.925 0.040 6 124238586 intron variant C/T snv 4.4E-02 2
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs5743611
TLR1
0.807 0.160 4 38798593 missense variant C/G snv 6.9E-02 7.1E-02 7
rs333
CCR5 ; CCR5AS
0.667 0.520 3 46373453 frameshift variant GTCAGTATCAATTCTGGAAGAATTTCCAGACA/- delins 7.3E-02 23
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1370967 0.925 0.040 5 111203694 intergenic variant G/A snv 7.8E-02 2
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs3826782
ADGRE1
0.882 0.040 19 6887725 intron variant G/A snv 8.6E-02 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs9446777
KCNQ5
1.000 0.040 6 72871328 intron variant A/G snv 9.2E-02 1