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
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 8
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 10
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 11
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 7
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 8
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs56131196
APOC1
0.925 0.160 19 44919589 downstream gene variant G/A snv 0.18 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9