Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs797044485
LMNA
0.851 0.160 1 156134832 missense variant G/A snv 4
rs879254597
LDLR
0.851 0.120 19 11105528 stop gained G/A;T snv 4
rs951599607
PPARG
0.925 0.040 3 12434028 missense variant G/A snv 4
rs2290602
PPARGC1A
0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs1420472625
MBOAT7
0.925 0.040 19 54178800 missense variant G/C snv 2
rs1346324047
LPA
1.000 0.040 6 160640717 missense variant G/A snv 1
rs940553638
ALDH2
0.827 0.200 12 111783222 missense variant G/A snv 1.6E-05 7.0E-06 6
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs748204991
ST14
1.000 0.040 11 130196396 missense variant G/A snv 2.1E-05 7.0E-06 1
rs772114791
PCSK9
1.000 0.040 1 55052343 missense variant G/A snv 8.0E-06 7.0E-06 1
rs74315468
ARSA
0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs11669576
LDLR ; MIR6886
0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 6
rs3213445
CHKB-CPT1B ; CPT1B
0.851 0.120 22 50577409 missense variant T/C snv 0.12 8.9E-02 4
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs56225452
SLC27A5 ; LOC105372486 ; ZBTB45
0.851 0.080 19 58513279 upstream gene variant C/T snv 0.18 5
rs12137855
LYPLAL1
0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 3
rs1010023
PNPLA3
0.851 0.080 22 43940218 intron variant T/C snv 0.20 4
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10