Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 4
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs61750929 9 88880220 regulatory region variant C/A;T snv 3
rs10820606 9 96430637 intergenic variant A/C snv 0.23 2
rs13042885 20 1944061 upstream gene variant C/A;T snv 2
rs1522744 15 64895675 intron variant C/G;T snv 2
rs1555405 14 100710432 regulatory region variant G/A snv 0.29 2
rs17568628 5 76751114 intergenic variant T/C;G snv 2
rs3002416 X 39850941 upstream gene variant C/T snv 0.33 2
rs35427 12 115118502 intergenic variant T/G snv 0.40 2
rs4699154 4 105112927 intron variant T/A;C snv 2
rs6756513 1.000 0.080 2 69945455 downstream gene variant G/A snv 0.26 2
rs7585866 2 191831529 downstream gene variant A/G snv 0.24 2
rs7616006 3 12226148 intergenic variant A/G snv 0.48 2
rs80012730 12 49277876 upstream gene variant A/C snv 6.1E-02 2
rs9809116 3 72348128 TF binding site variant A/G snv 0.51 2
rs9908158 17 35563064 upstream gene variant T/A;C snv 2
rs10757287 9 22143571 regulatory region variant A/T snv 0.22 1
rs10811664 9 22142908 regulatory region variant G/A snv 0.21 1
rs11240408 1 205295408 intergenic variant A/C;G;T snv 1
rs11446839 9 38198231 intergenic variant -/G delins 0.48 1