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
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs8071884
PGS1
17 78401977 intron variant C/A;G;T snv 4
rs11987974
LOC105379376
8 36966299 intergenic variant C/A;T snv 4
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs2954022 8 125470379 intron variant C/A;T snv 4
rs34630693
LRP1
12 57212472 missense variant C/A;T snv 1.2E-05; 2.0E-05 4
rs3794695
HPR ; TXNL4B
16 72063928 intron variant C/A;T snv 4
rs41274050
ASAH2B ; A1CF
10 50814012 missense variant C/A;T snv 4.0E-06; 5.3E-03 4
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs10761716 10 63122540 downstream gene variant C/G snv 0.40 3
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs2523575 6 31361049 upstream gene variant C/G snv 0.20 4
rs34614287
LRP1
12 57155352 3 prime UTR variant C/G snv 6.8E-04 4
rs35381288
ADRB3
8 37965106 non coding transcript exon variant C/G snv 7.4E-03 6
rs7333748
COL4A2
13 110366382 intron variant C/G snv 0.40 2
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs11569302
CD40
20 46118465 intron variant C/G;T snv 4
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs116477171
CYP21A2 ; C2
6 31918153 intron variant C/G;T snv 3
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 10
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8