Disease: Low density lipoprotein cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs17145738
TBL2
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 11
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 11
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11