Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs120074114
APOC2 ; APOC4-APOC2
19 44948767 missense variant A/C snv 6.9E-04 7.0E-04 2
rs1451659304
LMF1
1.000 0.040 16 868990 missense variant A/C snv 2
rs121918394
APOE
0.882 0.080 19 44908786 missense variant A/C;G snv 6.5E-06 5
rs615563
PCSK9
1.000 0.120 1 55060623 intron variant A/C;G snv 2
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 7
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs3819024
IL17A
0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 7
rs3828599
GPX3 ; LOC105378228
0.882 0.040 5 151022235 intron variant A/G snv 0.67 5
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 5
rs3862434
CRTC3
1.000 0.080 15 90537155 intron variant A/G snv 0.48 3
rs11122316
GALNT2
1.000 0.120 1 230101356 intron variant A/G snv 0.42 2
rs11634397 1.000 0.080 15 80139880 downstream gene variant A/G snv 0.57 2
rs2187126
BUD13
11 116765068 intron variant A/G snv 4.8E-02 2
rs957970
STAT3
1.000 0.040 17 42367872 intron variant A/G snv 0.36 2
rs12453407
ACACA
17 37232521 intron variant A/G snv 0.65 1
rs1266175
ACACA
17 37111115 intron variant A/G snv 0.54 1