Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17281995
CD86
0.763 0.360 3 122120794 3 prime UTR variant G/A;C snv 11
rs1915087
CD86
0.925 0.080 3 122119944 3 prime UTR variant T/C snv 2
rs2332096
CD86
0.925 0.080 3 122102296 intron variant T/A;G snv 2
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1475145065
CTSG
0.882 0.080 14 24574706 missense variant C/G;T snv 4.0E-06; 8.0E-06 3
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6
rs2839693
CXCL12
0.882 0.120 10 44379119 intron variant T/A;C snv 3
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs805305
DDAH2
0.882 0.120 6 31729610 intron variant C/G snv 0.48 3
rs1799946
DEFB1
0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs1554162524
ELOVL4
0.882 0.160 6 79925034 splice acceptor variant T/C snv 4
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 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
rs11666254
FPR2 ; FPR1
0.925 0.080 19 51759909 intron variant A/G snv 0.28 2
rs2808530
GABBR2
0.925 0.080 9 98576823 intron variant A/C snv 0.12 2
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19