Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267606661
APOE
0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs573658040
APOE
0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs1558861 11 116736721 regulatory region variant C/G;T snv 5
rs2297322
SLC15A1
1.000 0.040 13 98723927 missense variant C/G;T snv 0.22 4
rs59914820
LMNA
0.925 0.160 1 156115000 missense variant C/G;T snv 3
rs777407596
APOA1 ; APOA1-AS
11 116837145 missense variant C/G;T snv 4.0E-06 2
rs759009903
ACE
17 63484413 missense variant C/G;T snv 1.6E-05 1
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs3856806
PPARG
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs17145738
TBL2
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 11
rs118204060
LPL
0.807 0.160 8 19954279 missense variant C/T snv 4.0E-05 1.4E-05 9
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 8
rs46522
UBE2Z
0.807 0.120 17 48911235 non coding transcript exon variant C/T snv 0.40 8
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs2854116
APOC3
0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs2259820
HNF1A
0.882 0.160 12 120997539 synonymous variant C/T snv 0.34 0.26 6
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 4
rs633389 1.000 0.040 11 116796621 upstream gene variant C/T snv 0.13 4
rs2187331
LOC107984343
0.925 0.080 11 68678956 upstream gene variant C/T snv 0.84 3
rs2454727
HCAR2
0.925 0.040 12 122702333 missense variant C/T snv 3