Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs5888
SCARB1
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 9
rs3745367
RETN
0.827 0.200 19 7669625 intron variant G/A snv 0.39 8
rs5030718
TLR4
0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs2292318
SLC12A4
0.925 0.120 16 67951803 intron variant C/A;T snv 0.15 5