Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3135353 0.882 0.280 6 32425100 intergenic variant C/T snv 9.4E-02 3
rs412657 0.882 0.240 6 32243308 intergenic variant T/C;G snv 3
rs423639 0.882 0.240 6 33019997 intergenic variant C/T snv 0.11 3
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs7202877 0.882 0.160 16 75213347 intergenic variant T/C;G snv 3
rs7745656 0.882 0.200 6 32713193 upstream gene variant G/T snv 0.29 3
rs7755596 0.882 0.280 6 32738701 upstream gene variant C/T snv 0.80 3
rs7758736 0.882 0.200 6 32790617 intergenic variant G/A snv 0.14 3
rs7765379 0.827 0.280 6 32713151 upstream gene variant T/G snv 0.10 3
rs7773694 0.882 0.280 6 32738557 upstream gene variant A/G snv 0.80 3
rs9267649 0.882 0.240 6 31857051 downstream gene variant A/G snv 0.88 3
rs9267992 0.882 0.240 6 32252620 upstream gene variant G/A snv 0.89 3
rs9268528 0.851 0.280 6 32415331 regulatory region variant A/G snv 0.34 3
rs9268542 0.851 0.280 6 32416944 intergenic variant A/G snv 0.35 3
rs9268615 0.882 0.280 6 32435112 upstream gene variant G/A snv 0.38 3
rs9275184 0.882 0.200 6 32686937 regulatory region variant T/C snv 9.1E-02 3
rs9275328 0.851 0.240 6 32699045 intergenic variant C/T snv 0.16 3
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 3
rs9276162 0.882 0.280 6 32730680 downstream gene variant G/A snv 0.74 3
rs9276991 0.882 0.240 6 33014071 upstream gene variant A/G snv 6.0E-02 3
rs13199787 0.925 0.200 6 32737499 upstream gene variant C/T snv 0.38 2
rs1383265 0.925 0.200 6 32772111 intergenic variant T/A;C snv 2
rs1419675 1.000 0.120 6 30124930 intergenic variant G/T snv 0.74 2
rs154981 0.925 0.200 6 32913216 regulatory region variant C/A;G;T snv 2