Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10494326 1 159679910 intergenic variant C/T snv 5.3E-02 1
rs10521222 16 51124799 intergenic variant C/T snv 3.2E-02 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
rs11265260 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 1
rs11265263 1 159740727 intergenic variant C/A;T snv 1
rs12023742 1 19965513 intergenic variant C/A;G snv 1
rs12029262 1 159709406 upstream gene variant G/C snv 8.5E-02 1
rs12037222 1 39599289 regulatory region variant G/A snv 0.16 1
rs12093699 1 159678198 intergenic variant G/A;C snv 0.31 1
rs12408941 1 19958994 intergenic variant G/A snv 9.7E-02 1
rs12568139 1 19985183 upstream gene variant A/G snv 6.0E-02 1
rs12722987 1 20128727 intergenic variant C/A snv 0.17 1
rs12749227 1 159689319 intergenic variant C/T snv 0.25 1
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 1
rs12960928 1.000 0.080 18 60230570 intergenic variant T/C snv 0.21 1
rs12995480 2 629881 intergenic variant T/C snv 0.85 1
rs13375019 1 65657453 intergenic variant G/C;T snv 1
rs13375942 1 19965885 regulatory region variant T/A;C;G snv 1
rs13409371 2 113080568 downstream gene variant G/A;C;T snv 1
rs1341665 1.000 0.080 1 159721769 intergenic variant G/A snv 0.32 1
rs1408282 6 93142534 intergenic variant G/A snv 9.6E-02 1
rs149520992 1 159697727 intergenic variant C/T snv 3.8E-03 1
rs151233628 17 6258465 regulatory region variant C/G;T snv 1