Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10912533 1 173110803 intergenic variant C/T snv 0.76 1
rs10921464 1 193920403 intron variant C/A;T snv 1
rs10969844 9 30734469 intergenic variant A/T snv 0.49 1
rs10973047 9 36733409 intergenic variant A/G;T snv 1
rs10973048 9 36733481 intergenic variant G/A;C;T snv 1
rs10973049 9 36734290 intergenic variant T/C snv 0.58 1
rs10983710 9 117604336 intergenic variant C/T snv 1
rs11049850 12 28827505 upstream gene variant C/T snv 0.31 1
rs11049899 12 28890000 intergenic variant C/T snv 0.10 1
rs11050048 12 29120662 intergenic variant A/G snv 0.31 1
rs11050937 12 30515838 intergenic variant G/A snv 9.1E-02 1
rs11058598 12 126278221 intron variant C/T snv 2.4E-04 1
rs11058749 12 126611681 intron variant C/G snv 0.12 1
rs11070722 15 49815129 intergenic variant C/T snv 1.3E-02 1
rs11089258 22 19174763 downstream gene variant C/T snv 0.40 1
rs11102249 1 111322078 intron variant G/A snv 0.13 1
rs11117016 12 85747824 regulatory region variant T/A;C;G snv 1
rs11117017 12 85748062 regulatory region variant G/A;T snv 1
rs11117020 12 85748459 regulatory region variant C/T snv 0.67 1
rs11117021 12 85749846 intergenic variant C/A;T snv 1
rs11132005 4 180585282 intergenic variant T/A;G snv 1
rs11139265 9 81458709 intergenic variant T/C snv 5.0E-02 1
rs11139273 9 81477208 intergenic variant A/G snv 5.3E-02 1
rs11139275 9 81477586 regulatory region variant T/A snv 8.7E-02 1
rs11139278 9 81478174 intergenic variant T/G snv 5.3E-02 1