Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 7
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 6
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs62434129
PLEKHG1
6 150687701 intron variant A/G;T snv 8.8E-02 6
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 5
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5