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
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
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 7
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 6
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs1183910
HNF1A
1.000 0.080 12 120983004 intron variant G/A snv 0.28 5
rs1529711
CARM1
1.000 0.080 19 10912758 intron variant C/T snv 0.13 4
rs2287921
RASIP1
1.000 0.040 19 48725015 non coding transcript exon variant T/C snv 0.37 4
rs11220463
ST3GAL4
11 126378316 intron variant A/T snv 0.12 3
rs340005
RORA-AS1 ; RORA
15 60585831 intron variant G/A snv 0.67 3
rs3822857
FRK
6 115992768 intron variant G/A;C snv 3
rs4703642
LOC105379040
5 74966337 intron variant A/G snv 0.50 3
rs661955 1 234707109 upstream gene variant G/C;T snv 3
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
rs10744775
BRAP
12 111658411 intron variant T/C snv 0.44 2
rs12711751 2 113080188 downstream gene variant T/G snv 0.61 2
rs2285810
HECTD4
12 112261736 non coding transcript exon variant T/C snv 0.45 2