Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10437339 1 159740595 intergenic variant C/G;T snv 1
rs10437340 1 159741019 intergenic variant G/C snv 0.40 1
rs10489849 1 159226975 regulatory region variant C/A;T snv 1
rs10494326 1 159679910 intergenic variant C/T snv 5.3E-02 1
rs10521222 16 51124799 intergenic variant C/T snv 3.2E-02 1
rs10751037 11 81025386 intron variant C/G;T snv 1
rs10789192 1 65660087 intergenic variant G/A snv 0.43 1
rs10888935 1 55595278 intron variant T/A snv 0.52 1
rs10908733 1 159534264 downstream gene variant T/A;C snv 1
rs11108056 12 95461609 regulatory region variant C/G;T snv 1
rs111269058 7 73561372 upstream gene variant C/T snv 9.8E-02 1
rs1119582 5 125907327 intron variant T/C snv 1
rs11208711 1 65682163 intergenic variant G/T snv 0.43 1
rs11265177 1 159356044 intron variant A/G snv 0.16 1
rs11265180 1 159373858 intron variant G/C snv 0.11 1
rs11265218 1 159516850 intergenic variant T/C snv 9.9E-02 1
rs11265230 1 159545505 intergenic variant A/G snv 0.13 1
rs11265257 1 159699194 intergenic variant C/T snv 0.34 1
rs11265265 1 159743766 intergenic variant T/A;C snv 1
rs11588887 1 159747372 intergenic variant G/A snv 0.17 1
rs11661856 18 77941567 intergenic variant G/A snv 3.3E-02 1
rs11678375 2 113078114 downstream gene variant T/C snv 0.56 1
rs11697871 20 61218983 regulatory region variant T/C snv 0.58 1
rs11811256 1 159508440 intergenic variant T/C snv 0.46 1
rs11861089 16 77985790 intergenic variant T/C;G snv 1