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
rs16991720
KCNE1
21 34484464 intron variant A/C snv 4
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs11207995
DOCK7
1 62583880 intron variant A/C;G snv 4
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 5
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs10518982
LIPC
15 58507555 intron variant A/G snv 2.2E-02 3
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs11925396 3 194391622 downstream gene variant A/G snv 1.9E-02 3
rs12721054
APOC1
19 44919330 3 prime UTR variant A/G snv 3.7E-02 3
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs1713222 2 21048451 upstream gene variant A/G snv 0.82 3
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 7
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 8
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs193084249 1 26661155 intergenic variant A/G snv 1.7E-02 3
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs2249105
CEP68
2 65060762 intron variant A/G snv 0.40 5