Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17074636 0.925 0.120 4 183356978 regulatory region variant T/G snv 4.2E-02 1
rs2168303 0.925 0.120 18 60708701 intron variant A/G snv 2.9E-02 1
rs4148613
ABCC8
0.925 0.120 11 17454913 intron variant C/G snv 4.8E-03 1
rs3135753
FGFR2
0.925 0.120 10 121521144 intron variant T/C snv 4.0E-03 1
rs10002984 0.925 0.120 4 9679109 intron variant T/C snv 0.95 2
rs10005684 0.925 0.120 4 9625273 intron variant T/A;G snv 2
rs1000662 0.925 0.120 11 64466347 intergenic variant G/A snv 0.60 2
rs10007469 0.925 0.120 4 9731119 upstream gene variant G/A;C;T snv 2
rs10011621 0.925 0.120 4 9758615 downstream gene variant A/C snv 0.22 2
rs10022012 0.925 0.120 4 9691558 intron variant A/T snv 0.34 2
rs1003697 0.925 0.120 11 64466311 intergenic variant A/G;T snv 2
rs10049659 0.925 0.120 4 9585140 intron variant C/T snv 0.28 2
rs10049735 0.925 0.120 4 9624785 intron variant T/C snv 0.18 2
rs10087208 0.925 0.120 8 75850145 intergenic variant G/A snv 0.66 2
rs10155145 0.925 0.120 4 10127176 intergenic variant C/T snv 0.13 2
rs1035052 0.925 0.120 4 10343715 intergenic variant A/G snv 0.90 2
rs10458103 0.925 0.120 6 7037505 intergenic variant G/A snv 0.47 2
rs10489067 0.925 0.120 4 10338862 intergenic variant T/C snv 7.7E-02 2
rs10489074 0.925 0.120 4 10270981 upstream gene variant C/A;T snv 2
rs10516796 0.925 0.120 4 87935581 intergenic variant C/T snv 0.55 2
rs10516798 0.925 0.120 4 87962385 regulatory region variant T/C snv 0.42 2
rs10516800 0.925 0.120 4 87970438 downstream gene variant G/C snv 0.27 2
rs1060525 0.925 0.120 2 27412715 upstream gene variant A/G snv 0.48 2
rs1074155 0.925 0.120 11 65690726 upstream gene variant T/C snv 0.34 2
rs1074156 0.925 0.120 11 65690698 upstream gene variant G/T snv 0.34 2