Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs6894249
IRF1-AS1
0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45 9
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 8
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 8
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 8
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 7
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 7
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 7
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 7
rs679574
FUT2 ; LOC105447645
0.827 0.120 19 48702851 intron variant C/G snv 0.45 7