Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10032742 0.925 0.120 4 10277269 intergenic variant A/C;G;T snv 3
rs10033955 0.925 0.120 4 10176932 intergenic variant T/A;C snv 3
rs10034405 0.925 0.120 4 10172072 upstream gene variant A/G snv 0.14 3
rs1009144 0.925 0.120 4 10163307 downstream gene variant G/C;T snv 3
rs1017124 0.925 0.120 4 10248775 intergenic variant T/A;C snv 3
rs10489068 0.925 0.120 4 10285644 non coding transcript exon variant A/G;T snv 3
rs10489069 0.925 0.120 4 10277044 intergenic variant G/A;C;T snv 3
rs10489070 0.925 0.120 4 10274728 intergenic variant C/G snv 0.17 3
rs10489071 0.925 0.120 4 10271925 upstream gene variant G/A snv 0.68 3
rs10489072 0.925 0.120 4 10271620 upstream gene variant T/C snv 0.70 3
rs10489073 0.925 0.120 4 10271164 upstream gene variant G/A;C;T snv 3
rs10489076 0.925 0.120 4 10269224 upstream gene variant T/A;C snv 3
rs10489079 0.925 0.120 4 10202339 upstream gene variant G/C;T snv 0.18 3
rs10489080 0.925 0.120 4 10191803 regulatory region variant C/G;T snv 3
rs10516198 0.925 0.120 4 10057824 upstream gene variant T/C snv 0.15 3
rs10516201 0.925 0.120 4 10122317 intergenic variant T/C snv 0.18 3
rs10805356 0.925 0.120 4 10139978 downstream gene variant T/G snv 0.42 3
rs10805364 0.925 0.120 4 10273894 intergenic variant A/C;G snv 3
rs10910845 0.925 0.120 1 145711946 upstream gene variant T/G snv 0.44 3
rs10938768 0.925 0.120 4 10352717 intergenic variant C/A;T snv 3
rs10938772 0.925 0.120 4 10373704 intergenic variant A/G snv 0.19 3
rs10939507 0.925 0.120 4 9767199 downstream gene variant T/C snv 0.94 3
rs10939722 0.925 0.120 4 10137423 intergenic variant G/T snv 0.42 3
rs10939723 0.925 0.120 4 10137481 intergenic variant G/A;T snv 0.18 3
rs10939766 0.925 0.120 4 10203346 upstream gene variant A/G snv 0.66 3