Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs4986970
LCAT
0.925 0.080 16 67942417 missense variant A/C;T snv 4.0E-06; 1.7E-02 4
rs2351791
ATP10D
0.925 0.080 4 47580370 intron variant A/C;T snv 0.76 2
rs2271800
CYP2J2
1.000 0.080 1 59907994 intron variant A/C;T snv 1
rs6822035
SEC24D
1.000 0.080 4 118789266 intron variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31