Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008492 1.000 0.120 4 38764099 intergenic variant C/G;T snv 1
rs10024216 4 38762491 upstream gene variant G/A snv 0.37 1
rs10041894 5 40493132 intron variant G/A;C snv 1
rs10076944 5 40496849 intron variant G/A snv 0.60 1
rs10114457 9 6130940 intergenic variant A/G snv 0.81 1
rs10172116 2 102471113 upstream gene variant C/G;T snv 1
rs10181785 2 102408814 upstream gene variant C/T snv 0.22 1
rs10197310 2 102403570 downstream gene variant T/A snv 0.22 1
rs10202813 2 102403280 downstream gene variant G/T snv 0.22 1
rs10210176 2 102463056 intergenic variant C/A snv 0.22 1
rs1031163 10 9015459 regulatory region variant G/T snv 0.33 1
rs10447257 5 110845538 intergenic variant T/C;G snv 1
rs10470854 4 38766912 intergenic variant A/G snv 0.40 1
rs10497807 2 197720363 intron variant G/C snv 0.52 1
rs10793164 11 76431975 downstream gene variant A/T snv 0.40 1
rs10893845 11 128316987 regulatory region variant T/G snv 0.36 1
rs10899232 11 76568135 intergenic variant C/T snv 0.61 1
rs10931793 2 197712861 intron variant G/A snv 0.29 1
rs10947206 6 31393620 downstream gene variant A/T snv 0.31 1
rs10947332 6 32709663 upstream gene variant G/A snv 0.14 1
rs10957979 1.000 0.080 8 80377552 intron variant A/G snv 0.61 1
rs10975558 9 6364449 regulatory region variant C/T snv 0.21 1
rs11255965 10 8889830 intergenic variant G/A;T snv 3.9E-02 1
rs11255967 10 8891448 intergenic variant G/A snv 5.1E-02 1
rs11606100 11 76564534 regulatory region variant A/G;T snv 1