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
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 10
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
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
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs17789218
LOC105377911
6 100152221 intergenic variant T/A;C snv 3
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs1859287
SUGP1
19 19311378 intron variant T/A;C;G snv 4
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 10
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs2255141
GPAM
10 112174128 intron variant A/G;T snv 5
rs2304128
GMIP
19 19635342 intron variant G/C;T snv 5
rs2384034
RPH3A
12 112766880 intron variant C/G;T snv 4
rs2452170 19 48710247 downstream gene variant G/A;C snv 3
rs2954022 8 125470379 intron variant C/A;T snv 4
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs306890
SPRY3
Y 56944005 intergenic variant T/C snv 4
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs34499590
LEPR
1 65616108 missense variant C/G;T snv 2.5E-03 3
rs34630693
LRP1
12 57212472 missense variant C/A;T snv 1.2E-05; 2.0E-05 4