Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10087900 8 143221248 downstream gene variant G/A snv 0.37 1
rs10091038 8 29502788 intergenic variant A/C snv 0.57 1
rs10198423 2 85333439 upstream gene variant G/A;C;T snv 1
rs1026422 7 50280211 upstream gene variant G/A snv 0.51 1
rs10479024 5 133131681 intergenic variant C/A;T snv 1
rs10836699 11 37162788 intergenic variant C/T snv 0.33 1
rs1084651 6 160668785 intron variant G/A snv 0.23 1
rs10874777 1 93396463 intergenic variant T/A;C snv 1
rs11045163 12 20310592 intergenic variant A/G snv 0.38 1
rs11045171 12 20317265 intergenic variant A/G snv 0.16 1
rs11067829 12 109679067 regulatory region variant A/G snv 0.23 1
rs11082766 18 49606094 intergenic variant C/T snv 4.4E-02 1
rs11218720 11 122633992 intergenic variant A/G snv 0.39 1
rs11236520 11 75749624 intergenic variant G/A snv 0.11 1
rs11246602 11 54607190 upstream gene variant A/G snv 0.11 1
rs11434755 11 18045473 upstream gene variant -/A delins 0.41 1
rs114529226 14 106368436 upstream gene variant G/A snv 4.3E-02 1
rs116569761 6 32680379 intergenic variant G/A snv 1
rs11782435 8 13678606 intergenic variant C/T snv 0.16 1
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 1
rs12226802 11 55556832 downstream gene variant A/G snv 0.10 1
rs12575459 11 58394909 regulatory region variant G/A snv 5.2E-02 1
rs1263173 0.925 0.080 11 116810292 downstream gene variant G/A snv 0.53 1
rs12740061 1 68942127 intron variant C/A;T snv 1
rs1281955 6 153138309 intergenic variant T/A snv 0.43 1