Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs2306283
SLCO1B1
0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
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
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06 8
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv 7
rs200960801
ESR1
0.827 0.200 6 151944488 missense variant A/G snv 4.0E-06 6
rs121964971
CBS
0.851 0.160 21 43058215 missense variant G/A snv 1.2E-05 5
rs150599989
C5AR2
0.827 0.320 19 47341767 missense variant G/A;C;T snv 4.0E-06; 9.6E-05 5
rs879254840
LDLR ; MIR6886
0.827 0.120 19 11113322 missense variant A/G snv 5
rs198388
NPPB
0.851 0.160 1 11857283 downstream gene variant C/G;T snv 4
rs4713518
TSBP1 ; TSBP1-AS1
0.925 0.160 6 32289560 intron variant A/G;T snv 3
rs6078
LIPC
0.882 0.120 15 58541794 missense variant G/A;T snv 7.1E-02; 8.0E-06 3
rs920435389
FGFR4
1.000 0.040 5 177091064 missense variant G/C snv 3
rs1251035592
CYP3A5 ; ZSCAN25
1.000 0.040 7 99664039 missense variant T/C snv 4.2E-06 1
rs1341991169
LPL
1.000 0.040 8 19939444 missense variant G/A snv 1
rs1444332461
ARSA
1.000 0.040 22 50627185 missense variant A/G snv 4.1E-06 1
rs3829462
LIPC
1.000 0.040 15 58560880 missense variant C/A;T snv 0.97 1
rs886916693
KIDINS220
1.000 0.040 2 8806360 missense variant T/C snv 4.1E-06 1
rs974389711
APOA1 ; APOA1-AS
1.000 0.040 11 116836210 synonymous variant C/T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614