Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10771462 1.000 0.080 12 29004395 intergenic variant G/A snv 0.82 1
rs10843003 1.000 0.080 12 27834007 intergenic variant T/G snv 0.14 1
rs10903128 1.000 0.080 1 25036847 upstream gene variant A/G snv 0.68 1
rs10919382 1.000 0.080 1 170392023 intergenic variant A/G snv 0.36 1
rs11049231 1.000 0.080 12 27938767 upstream gene variant G/A snv 4.6E-02 1
rs112069404 1.000 0.080 X 66331306 intergenic variant C/A;T snv 1
rs112348497 1.000 0.080 21 43207769 intergenic variant -/C delins 0.20 1
rs112949019 1.000 0.080 12 130078675 intergenic variant C/- del 0.24 1
rs113222435 1.000 0.080 X 67743865 intergenic variant G/T snv 2.5E-02 1
rs114190032 1.000 0.080 6 9509023 intergenic variant G/T snv 0.36 1
rs11497798 1.000 0.080 10 76617412 intergenic variant C/T snv 0.53 1
rs115176171 1.000 0.080 1 25006643 intergenic variant A/G snv 6.7E-02 1
rs115282290 1.000 0.080 1 204009986 downstream gene variant C/G;T snv 1
rs11586871 1.000 0.080 1 25073178 intron variant C/T snv 0.15 1
rs11594897 1.000 0.080 10 76617815 intergenic variant T/A;C;G snv 1
rs11759950 1.000 0.080 6 10226000 downstream gene variant C/T snv 0.15 1
rs117769774 1.000 0.080 8 108090690 intergenic variant G/A snv 2.5E-02 1
rs1195215 1.000 0.080 7 69271106 intron variant C/T snv 0.45 1
rs12077761 1.000 0.080 1 25082765 intron variant A/G snv 0.21 1
rs12326164 1.000 0.080 18 45096963 intergenic variant A/G snv 0.66 1
rs12472159 1.000 0.080 2 176826815 downstream gene variant C/G;T snv 1
rs12509636 1.000 0.080 4 105089276 intron variant C/T snv 0.39 1
rs12540951 1.000 0.080 7 69158905 intron variant G/A snv 0.17 1
rs12745121 1.000 0.080 1 25141389 regulatory region variant G/A snv 0.23 1
rs1351637 1.000 0.080 5 44441601 regulatory region variant A/G snv 0.17 1