Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs11618989 13 109836805 regulatory region variant C/T snv 7.8E-02 1
rs11628318 14 102573750 regulatory region variant T/A;C snv 1
rs11734099 4 6889708 intergenic variant G/A snv 0.14 1
rs11841319 13 109840279 regulatory region variant C/T snv 7.8E-02 1
rs11957129 5 178183210 downstream gene variant C/A;G;T snv 1
rs12005199 9 4763491 downstream gene variant G/A snv 0.27 1
rs12458093 18 51152780 intergenic variant T/G snv 0.40 1
rs141573810 6 130821850 intergenic variant AA/-;A;AAA;AAAA delins 0.45 1
rs141749350 4 54534440 intergenic variant A/G;T snv 1
rs147310751 22 19700711 intergenic variant A/T snv 1.0E-02 1
rs150568286 17 44517387 intergenic variant G/A snv 9.2E-03 1
rs1506636 7 123677086 downstream gene variant A/G;T snv 1
rs1631677 15 64906392 intron variant A/G snv 0.19 1
rs1719271 15 64891602 intron variant A/G snv 0.20 1
rs191021045 14 69022339 downstream gene variant C/T snv 1.3E-03 1
rs2316806 9 88861685 intergenic variant T/C snv 0.25 1
rs2546979 5 160168605 intergenic variant G/A;C snv 1
rs2700937 7 36045451 intron variant A/T snv 0.54 1
rs28550009 3 184371199 downstream gene variant A/G snv 0.15 1
rs2862064 5 157018816 intergenic variant C/A;G snv 1
rs290268 9 90790168 regulatory region variant A/G snv 0.40 1