Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986970
LCAT
0.925 0.080 16 67942417 missense variant A/C;T snv 4.0E-06; 1.7E-02 2
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs11974409
TBL2
0.925 0.120 7 73575060 intron variant A/G snv 0.16 6
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 6
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs261338
LIPC ; LIPC-AS1 ; ALDH1A2
15 58442806 intron variant A/G snv 0.83 5
rs3731215
CDKN2A
9 21985772 intron variant A/G snv 1.2E-03 5
rs4253642
LOC105373074 ; PPARA
22 46167520 intron variant A/G snv 7.1E-03 5
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93 5