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
rs2159324
BLOC1S3 ; MARK4
19 45192480 intron variant T/C snv 0.36 2
rs3999089
JMJD1C
10 63444048 intron variant A/G snv 0.41 2
rs6062343
TCEA2
20 64064578 intron variant G/A snv 0.44 2
rs6602911
GAS6-AS1 ; GAS6
13 113844399 non coding transcript exon variant C/T snv 0.48 2
rs7333748
COL4A2
13 110366382 intron variant C/G snv 0.40 2
rs7902343
JMJD1C
10 63245639 intron variant C/T snv 0.40 2
rs10504062
PRKDC
8 47824663 intron variant T/C snv 2.1E-02 3
rs10518982
LIPC
15 58507555 intron variant A/G snv 2.2E-02 3
rs10761716 10 63122540 downstream gene variant C/G snv 0.40 3
rs10957054
UBXN2B
8 58423997 intron variant C/T snv 0.73 3
rs10986881
PBX3
9 125756807 intron variant C/T snv 1.8E-02 3
rs11193085
SORCS1
10 106873848 intron variant G/A snv 8.8E-02 3
rs115485095
CYP21A2 ; EHMT2
6 31888293 intron variant G/A snv 3
rs11574728
CD36
7 80676025 intron variant G/A snv 7.5E-03 3
rs115845232
LOC112267902 ; HLA-B
6 31304484 intron variant C/T snv 3
rs116477171
CYP21A2 ; C2
6 31918153 intron variant C/G;T snv 3
rs11925396 3 194391622 downstream gene variant A/G snv 1.9E-02 3
rs12708979
CETP
16 56978442 intron variant C/T snv 5.9E-03 3
rs12721054
APOC1
19 44919330 3 prime UTR variant A/G snv 3.7E-02 3
rs1553318
HAVCR1
5 157052312 intron variant G/A;C snv 6.2E-03; 0.67 3
rs16940391
LIPC
15 58507449 intron variant C/A;G snv 3
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
rs17789218
LOC105377911
6 100152221 intergenic variant T/A;C snv 3
rs193084249 1 26661155 intergenic variant A/G snv 1.7E-02 3