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
rs17789218
LOC105377911
6 100152221 intergenic variant T/A;C snv 3
rs17883880
CHUK
10 100230590 intron variant T/A snv 1.2E-02 4
rs8071787
GAS7
17 10058819 intron variant T/C snv 4.8E-02 5
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 6
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs11193085
SORCS1
10 106873848 intron variant G/A snv 8.8E-02 3
rs585362 1 109247173 upstream gene variant C/G;T snv 4
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 8
rs611917
CELSR2
1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32 5
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs661171
ZC3H12C ; RDX
11 110145794 intron variant T/G snv 0.69 5
rs7333748
COL4A2
13 110366382 intron variant C/G snv 0.40 2
rs5985471 X 110460733 downstream gene variant C/T snv 0.43 4
rs5942937 X 110473179 intron variant T/G snv 0.47 4
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5