Disease: Serum LDL cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs10415849
GATAD2A
19 19394278 intron variant C/T snv 0.12 4
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs10500212
PBX4
19 19612406 intron variant C/T snv 0.10 4
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
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
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
rs11207997
DOCK7 ; ANGPTL3
1 62596235 intron variant C/T snv 0.39 6
rs11465759
IL23R ; C1orf141
1 67166721 intron variant T/G snv 2.4E-02 4
rs11466654
TLR10
4 38774508 synonymous variant T/C;G snv 1.1E-03; 1.8E-05 4
rs11568607
ABCC3
17 50668426 splice region variant G/A snv 7.4E-03 2.6E-02 4
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs11569302
CD40
20 46118465 intron variant C/G;T snv 4
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs11574728
CD36
7 80676025 intron variant G/A snv 7.5E-03 3
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 6
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5