Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1013443 5 180774114 intergenic variant A/T snv 1.4E-03 1
rs10958725 8 42669441 intergenic variant T/G snv 0.63 1
rs10958726 8 42680766 intergenic variant G/T snv 0.66 1
rs11071927 15 66968834 intergenic variant C/A snv 0.85 1
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 1
rs12461383 19 40864433 intron variant C/G snv 0.42 1
rs13273442 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 1
rs1383634 15 78737054 downstream gene variant T/C snv 0.53 1
rs1443512 12 53948900 downstream gene variant A/C;T snv 1
rs1451239 8 42691399 intergenic variant G/A;T snv 1
rs1496402 19 40860229 intron variant T/A snv 0.67 1
rs1678618 10 72046530 intergenic variant A/G snv 0.39 1
rs1776897 6 34227234 regulatory region variant G/T snv 0.80 1
rs1979140 8 42675693 intergenic variant T/C snv 0.63 1
rs2219939 1.000 0.040 15 78737381 downstream gene variant G/A snv 0.53 1
rs2568500 15 78434586 upstream gene variant C/T snv 0.46 1
rs2869030 15 78419461 regulatory region variant G/T snv 0.66 1
rs2869032 15 78422219 regulatory region variant C/G;T snv 1
rs2869045 15 78426557 regulatory region variant T/C snv 0.78 1
rs3025343 9 133613233 non coding transcript exon variant G/A snv 7.0E-02 1
rs34325700 8 42673524 intergenic variant -/A delins 1
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 1
rs4275821 15 78557199 downstream gene variant C/T snv 0.69 1
rs4343391 19 40838463 intron variant G/C snv 0.72 1
rs4362358 15 78503762 upstream gene variant C/T snv 0.50 1