Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 7
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 7
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 7
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs283813
NECTIN2
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16 6
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs519113
NECTIN2
1.000 0.080 19 44873027 intron variant C/G;T snv 6
rs6982636 8 125467073 intron variant G/A snv 0.43 6
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6