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
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs10415849
GATAD2A
19 19394278 intron variant C/T snv 0.12 4
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs10500212
PBX4
19 19612406 intron variant C/T snv 0.10 4
rs10504062
PRKDC
8 47824663 intron variant T/C snv 2.1E-02 3
rs10518982
LIPC
15 58507555 intron variant A/G snv 2.2E-02 3
rs10761716 10 63122540 downstream gene variant C/G snv 0.40 3
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs10876041
DIP2B
12 50508099 intron variant T/C snv 0.58 4
rs10889348
DOCK7
1 62612551 intron variant A/T snv 0.32 4
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 5
rs10900522
NUCKS1
1 205714939 3 prime UTR variant T/C snv 0.21 4
rs10957054
UBXN2B
8 58423997 intron variant C/T snv 0.73 3
rs10986881
PBX3
9 125756807 intron variant C/T snv 1.8E-02 3
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs11079810
SKAP1
17 48150484 intron variant C/T snv 0.16 4