Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34 6
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 6
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 6
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 5
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 5
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 5