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
rs2297991
GPAM
10 112153464 3 prime UTR variant T/C snv 0.69 4
rs77147124
GPAM
10 112159366 intron variant A/G snv 4
rs2255141
GPAM
10 112174128 intron variant A/G;T snv 5
rs2803621
GPAM
10 112179826 intron variant G/A snv 0.74 4
rs7096937
GPAM
10 112190660 intron variant T/C snv 0.72 5
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs2384034
RPH3A
12 112766880 intron variant C/G;T snv 4
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs6602911
GAS6-AS1 ; GAS6
13 113844399 non coding transcript exon variant C/T snv 0.48 2
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs509728 11 116662450 downstream gene variant G/C snv 2.7E-02 5
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 5
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 10
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs17120434
PCSK7 ; TAGLN
11 117204969 3 prime UTR variant A/G;T snv 5.4E-02 3
rs9658465
NOS1
12 117247093 intron variant T/G snv 2.3E-02 3
rs9658292
NOS1
12 117318980 intron variant G/C snv 9.4E-04 5
rs895953
SETD1B
1.000 0.040 12 121811142 intron variant G/T snv 0.76 5
rs2062432
ADCY5
3 123359232 intron variant G/A snv 0.43 4
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9