Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7