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
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
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
rs150641967
HAPLN4
19 19259532 intron variant AGAC/-;AGACAGAC delins 4
rs1553318
HAVCR1
5 157052312 intron variant G/A;C snv 6.2E-03; 0.67 3
rs1565228
BDNF-AS
11 27564889 intron variant G/A;C snv 4
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
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
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34 7
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28 6
rs1748197
DOCK7
1 62590441 intron variant G/A snv 0.42 5
rs176813 4 68733813 regulatory region variant T/C snv 0.38 4
rs17789218
LOC105377911
6 100152221 intergenic variant T/A;C snv 3
rs17883880
CHUK
10 100230590 intron variant T/A snv 1.2E-02 4