Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 8
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 7
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
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
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-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
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6