Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4756996 11 19333933 intergenic variant C/T snv 0.21 1
rs484084 1 234721929 upstream gene variant T/C snv 0.66 1
rs506585 2 21174310 intergenic variant G/A;C;T snv 1
rs537526354 4 72625905 intergenic variant G/A snv 1.5E-03 1
rs548145 2 21068440 regulatory region variant T/C snv 0.68 1
rs553427 1 234717013 intron variant C/T snv 0.65 1
rs56167574 7 151548889 intergenic variant G/A snv 5.4E-02 1
rs577584 2 21076995 intergenic variant T/A snv 0.68 1
rs58198139 5 156972028 intergenic variant C/G;T snv 1
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 1
rs6016381 20 40551796 regulatory region variant T/C snv 0.40 1
rs66883945 6 138996690 regulatory region variant -/C;CC delins 1
rs6982636 8 125467073 intron variant G/A snv 0.43 1
rs72834327 2 117842293 downstream gene variant A/T snv 5.7E-02 1
rs73219351 2 17295273 intergenic variant T/C;G snv 1
rs75214121 8 58485717 downstream gene variant C/T snv 2.5E-02 1
rs7523141 1 55033125 intergenic variant C/A;T snv 1
rs7538216 1 16183176 intergenic variant T/A;C snv 1
rs7569328 1.000 0.040 2 20901018 intergenic variant C/T snv 5.7E-02 1
rs7575840 1.000 0.040 2 21050618 intergenic variant G/T snv 0.26 1
rs77645768 4 72803111 upstream gene variant G/A snv 1.8E-02 1
rs79316815 1 2902742 intergenic variant A/G snv 9.2E-02 1
rs79588679 18 22327807 intergenic variant C/T snv 0.11 1
rs79950627 11 2212560 intergenic variant G/A snv 2.1E-02 1
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 1