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
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10744775
BRAP
12 111658411 intron variant T/C snv 0.44 2
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs11220463
ST3GAL4
11 126378316 intron variant A/T snv 0.12 3
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 6
rs1183910
HNF1A
1.000 0.080 12 120983004 intron variant G/A snv 0.28 5
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs1529711
CARM1
1.000 0.080 19 10912758 intron variant C/T snv 0.13 4
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 9
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs340005
RORA-AS1 ; RORA
15 60585831 intron variant G/A snv 0.67 3
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 7
rs3822857
FRK
6 115992768 intron variant G/A;C snv 3
rs4703642
LOC105379040
5 74966337 intron variant A/G snv 0.50 3
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
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
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29