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
rs3822857
FRK
6 115992768 intron variant G/A;C snv 3
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4703642
LOC105379040
5 74966337 intron variant A/G snv 0.50 3
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs661955 1 234707109 upstream gene variant G/C;T snv 3
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 11
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs8180991 8 125488108 intron variant C/G snv 0.19 3
rs9275292 1.000 0.120 6 32695512 intergenic variant C/A snv 0.53 3
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10