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
rs12258934
NRG3
10 82015079 intron variant T/C snv 5.1E-02 4
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 5
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs12610185
PBX4
19 19610913 intron variant G/A snv 8.6E-02 4
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 5
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 6
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
rs12721054
APOC1
19 44919330 3 prime UTR variant A/G snv 3.7E-02 3
rs12721235
AGTR1
3 148722587 intron variant C/A snv 1.7E-02 4
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 6
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs13392272 2 20994618 downstream gene variant C/T snv 0.37 5
rs1456649
FMN2
1 240288305 intron variant G/C snv 3.0E-03 5
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs150641967
HAPLN4
19 19259532 intron variant AGAC/-;AGACAGAC delins 4
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs1565228
BDNF-AS
11 27564889 intron variant G/A;C snv 4
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
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
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 8