Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs118204060
LPL
0.807 0.160 8 19954279 missense variant C/T snv 4.0E-05 1.4E-05 9
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs120074114
APOC2 ; APOC4-APOC2
19 44948767 missense variant A/C snv 6.9E-04 7.0E-04 2
rs121909397
LMF1
0.925 0.080 16 869982 stop gained G/A;C snv 1.6E-04; 4.0E-06 3
rs121918393
APOE
0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs121918394
APOE
0.882 0.080 19 44908786 missense variant A/C;G snv 6.5E-06 5
rs12453407
ACACA
17 37232521 intron variant A/G snv 0.65 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs1263163 11 116802796 intergenic variant G/A snv 0.10 2
rs1266175
ACACA
17 37111115 intron variant A/G snv 0.54 1
rs1289389
SLC15A1
13 98684036 3 prime UTR variant C/T snv 0.18 2
rs1335550286
APOE
1.000 0.040 19 44909005 missense variant G/A snv 7.0E-06 2
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs1378577
ABCG1
1.000 0.080 21 42199555 upstream gene variant T/G snv 0.33 2
rs140808909
APOE
0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05 5
rs1414423445
CREB3L3
19 4171402 stop gained C/A;T snv 4.0E-06; 4.0E-06 1
rs143292359
ZPR1 ; APOA5
11 116790285 missense variant G/A snv 5.9E-04 5.0E-04 1
rs1451659304
LMF1
1.000 0.040 16 868990 missense variant A/C snv 2
rs145657341
LPL
0.925 0.120 8 19951811 missense variant G/A snv 1.7E-04 7.0E-05 3
rs146515657
USP4
3 49292533 missense variant T/C snv 1.1E-04 3.1E-04 1
rs1468271
LOC107986777 ; NPY
1.000 0.040 7 24287362 intron variant C/T snv 0.97 2
rs149089920
LPL
0.925 0.120 8 19962134 missense variant G/A snv 6.0E-05 2.1E-04 3
rs149808404
APOA5 ; ZPR1
11 116790406 stop gained G/A;C snv 4.1E-05; 8.1E-06 1
rs1558861 11 116736721 regulatory region variant C/G;T snv 5