Disease: Low density lipoprotein cholesterol measurement
Source: GWASDB ×
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 6
rs11465759
IL23R ; C1orf141
1 67166721 intron variant T/G snv 2.4E-02 4
rs2829976
APP
21 25900162 intron variant T/G snv 3.6E-02 3
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
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
rs531819
APOB
2 21040767 intron variant T/G snv 0.83 3
rs570877
APOB
2 21028168 intron variant T/G snv 0.87 3
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs6453131
HMGCR
5 75348881 intron variant T/G snv 0.39 3
rs754524 2 21088669 intergenic variant T/G snv 0.19 4
rs8104483
NECTIN2
19 44869097 intron variant T/G snv 0.28 3
rs11466654
TLR10
4 38774508 synonymous variant T/C;G snv 1.1E-03; 1.8E-05 4
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 3
rs4722551
LOC105375199
7 25952206 upstream gene variant T/C;G snv 4
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 10
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs11568373
ABCB11
2 168944893 synonymous variant T/C snv 5.8E-03 2.6E-02 3
rs11868655
NLRP1
17 5522873 intron variant T/C snv 2.3E-02 3
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 4
rs12720826
APOB
2 21042823 intron variant T/C snv 3.8E-02 3
rs12720900
CETP
16 56977385 non coding transcript exon variant T/C snv 8.9E-04 3
rs1564348
SLC22A1
6 160157828 intron variant T/C snv 0.14 3