Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2356864 1 50374068 intergenic variant G/A snv 0.51 1
rs2436962 8 102633585 intergenic variant A/G snv 0.87 1
rs2480712 1 2225560 upstream gene variant G/C;T snv 1
rs2573674 15 99936478 intergenic variant C/A snv 0.28 1
rs2581360 15 99951677 regulatory region variant C/T snv 0.28 1
rs2760215 1 163706152 regulatory region variant T/C snv 0.43 1
rs2941487 8 75568115 downstream gene variant T/C snv 0.54 1
rs2970581 1 211910170 regulatory region variant G/A snv 2.7E-02 1
rs3118365 6 28872131 regulatory region variant G/A;C snv 1
rs35501037 6 27771787 intergenic variant T/A snv 5.6E-02 1
rs4077450 16 79897698 TF binding site variant G/T snv 0.74 1
rs4077451 16 79897823 TF binding site variant T/A;C snv 1
rs4246529 1 155142784 upstream gene variant T/C snv 0.42 1
rs4724828 7 1258812 intergenic variant C/G;T snv 1
rs4889855 17 80539480 upstream gene variant G/A snv 0.85 1
rs531763 11 64584591 intergenic variant A/G snv 0.45 1
rs56106601 9 128008205 intergenic variant A/C snv 9.4E-02 1
rs56129505 1 186749129 intergenic variant C/T snv 0.25 1
rs57629029 4 10484718 intron variant T/C snv 0.21 1
rs59420943 4 10382654 intergenic variant C/A;T snv 1
rs62128132 19 49714698 downstream gene variant T/C snv 2.3E-02 1
rs62286563 4 10121041 upstream gene variant T/C;G snv 1
rs62517932 8 76119358 intergenic variant G/A snv 6.9E-02 1
rs6445559 3 53065450 intron variant A/G;T snv 1
rs6460047 7 73628113 upstream gene variant T/C snv 0.22 1