Disease: Serum LDL cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11925396 3 194391622 downstream gene variant A/G snv 1.9E-02 3
rs12258934
NRG3
10 82015079 intron variant T/C snv 5.1E-02 4
rs12610185
PBX4
19 19610913 intron variant G/A snv 8.6E-02 4
rs12708979
CETP
16 56978442 intron variant C/T snv 5.9E-03 3
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs12721235
AGTR1
3 148722587 intron variant C/A snv 1.7E-02 4
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 5
rs1456649
FMN2
1 240288305 intron variant G/C snv 3.0E-03 5
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs16880248
CNR1
6 88141968 3 prime UTR variant G/T snv 2.7E-02 5
rs16940391
LIPC
15 58507449 intron variant C/A;G snv 3
rs16957552
BCAR1
16 75235226 missense variant T/C snv 6.8E-03 2.8E-02 4
rs16991720
KCNE1
21 34484464 intron variant A/C snv 4
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 5
rs17031710
ABCG8 ; LOC102725159
2 43843754 intron variant A/T snv 2.1E-02 4
rs17120434
PCSK7 ; TAGLN
11 117204969 3 prime UTR variant A/G;T snv 5.4E-02 3
rs1713222 2 21048451 upstream gene variant A/G snv 0.82 3
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 9
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9