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
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs11465759
IL23R ; C1orf141
1 67166721 intron variant T/G snv 2.4E-02 4
rs3850634
DOCK7
1 62584927 intron variant T/G snv 0.33 0.34 4
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs4495740
DOCK7
1 62658794 intron variant T/G snv 0.34 5
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04 6
rs5185
AGTR1
3 148742185 3 prime UTR variant T/G snv 6.7E-03 2.5E-02 4
rs5942937 X 110473179 intron variant T/G snv 0.47 4
rs661171
ZC3H12C ; RDX
11 110145794 intron variant T/G snv 0.69 5
rs754524 2 21088669 intergenic variant T/G snv 0.19 4
rs9658465
NOS1
12 117247093 intron variant T/G snv 2.3E-02 3
rs11466654
TLR10
4 38774508 synonymous variant T/C;G snv 1.1E-03; 1.8E-05 4
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs4722551
LOC105375199
7 25952206 upstream gene variant T/C;G snv 5
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 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
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs10504062
PRKDC
8 47824663 intron variant T/C snv 2.1E-02 3
rs10876041
DIP2B
12 50508099 intron variant T/C snv 0.58 4
rs10900522
NUCKS1
1 205714939 3 prime UTR variant T/C snv 0.21 4
rs12258934
NRG3
10 82015079 intron variant T/C snv 5.1E-02 4
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 5
rs16957552
BCAR1
16 75235226 missense variant T/C snv 6.8E-03 2.8E-02 4