Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs2229738
CPT1A
11 68794860 missense variant C/G;T snv 6.3E-02 2
rs17610395
CPT1A
11 68794860 missense variant C/G;T snv 1
rs186183604
RAD9A ; LOC100130987
11 67361262 intron variant G/A;T snv 1
rs17267292
GPC5 ; LOC105370315
13 92670893 intron variant T/C snv 0.22 2
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs35853021
ALDH1A2
15 58388444 intron variant G/T snv 0.38 1
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 10
rs7499892
CETP
16 56972678 intron variant C/G;T snv 7
rs11644601
RRN3 ; PDXDC1
16 15078261 intron variant T/C snv 0.21 4
rs11075253
PDXDC1 ; NTAN1
16 15054789 intron variant C/A snv 0.22 1
rs181807530
MINK1
17 4871519 intron variant C/G snv 4.8E-03 1
rs4939883
LOC105372112
1.000 0.040 18 49640844 TF binding site variant T/C;G snv 5
rs7228085
LOC105372112
18 49634444 intergenic variant A/G snv 0.53 1
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 6
rs17249141
LDLR
19 11089332 upstream gene variant C/T snv 3.3E-03 4
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 3